Human Secreted Proteins

ABSTRACT

The present invention relates to human secreted polypeptides, and isolated nucleic acid molecules encoding said polypeptides, useful for diagnosing and treating cancer and other hyperproliferative diseases and disorders. Antibodies that bind these polypeptides are also encompassed by the present invention. Also encompassed by the invention are vectors, host cells, and recombinant and synthetic methods for producing said polynucleotides, polypeptides, and/or antibodies. The invention further encompasses screening methods for identifying agonists and antagonists of polynucleotides and polypeptides of the invention. The present invention further encompasses methods and compositions for inhibiting or enhancing the production and function of the polypeptides of the present invention.

RELATED APPLICATIONS

This application is a division of U.S. patent application Ser. No. 10/664,356, filed Sep. 20, 2003, which is a continuation-in-part of PCT/US02/08123, filed Mar. 19, 2002, which in turn claims benefit of the following: Application:: Continuity Type:: Parent Application:: Parent Filing Date:: PCT/US02/08123 Continuation-in-part of 10/100,683 Mar. 19, 2002 10/100,683 Non-provisional of 60/277,340 Mar. 21, 2001 10/100,683 Non-provisional of 60/306,171 Jul. 19, 2001 10/100,683 Non-provisional of 60/331,287 Nov. 13, 2001 10/100,683 Continuation-in-part of 09/981,876 Oct. 19, 2001 09/981,876 Divisional of 09/621,011 Jul. 20, 2000 09/621,011 Continuation of 09/148,545 Sep. 04, 1998 09/148,545 Continuation-in-part of PCT/US98/04482 Mar. 06, 1998 10/100,683 Continuation-in-part of 09/621,011 Jul. 20, 2000 09/621,011 Continuation of 09/148,545 Sep. 04, 1998 09/148,545 Continuation-in-part of PCT/US98/04482 Mar. 06, 1998 10/100,683 Continuation-in-part of 09/148,545 Sep. 04, 1998 09/148,545 Continuation-in-part of PCT/US98/04482 Mar. 06, 1998 10/100,683 Continuation-in-part of PCT/US98/04482 Mar. 06, 1998 PCT/US98/04482 Non-provisional of 60/040,162 Mar. 07, 1997 PCT/US98/04482 Non-provisional of 60/040,333 Mar. 07, 1997 PCT/US98/04482 Non-provisional of 60/038,621 Mar. 07, 1997 PCT/US98/04482 Non-provisional of 60/040,161 Mar. 07, 1997 PCT/US98/04482 Non-provisional of 60/040,626 Mar. 07, 1997 PCT/US98/04482 Non-provisional of 60/040,334 Mar. 07, 1997 PCT/US98/04482 Non-provisional of 60/040,336 Mar. 07, 1997 PCT/US98/04482 Non-provisional of 60/040,163 Mar. 07, 1997 PCT/US98/04482 Non-provisional of 60/047,615 May 23, 1997 PCT/US98/04482 Non-provisional of 60/047,600 May 23, 1997 PCT/US98/04482 Non-provisional of 60/047,597 May 23, 1997 PCT/US98/04482 Non-provisional of 60/047,502 May 23, 1997 PCT/US98/04482 Non-provisional of 60/047,633 May 23, 1997 PCT/US98/04482 Non-provisional of 60/047,583 May 23, 1997 PCT/US98/04482 Non-provisional of 60/047,617 May 23, 1997 PCT/US98/04482 Non-provisional of 60/047,618 May 23, 1997 PCT/US98/04482 Non-provisional of 60/047,503 May 23, 1997 PCT/US98/04482 Non-provisional of 60/047,592 May 23, 1997 PCT/US98/04482 Non-provisional of 60/047,581 May 23, 1997 PCT/US98/04482 Non-provisional of 60/047,584 May 23, 1997 PCT/US98/04482 Non-provisional of 60/047,500 May 23, 1997 PCT/US98/04482 Non-provisional of 60/047,587 May 23, 1997 PCT/US98/04482 Non-provisional of 60/047,492 May 23, 1997 PCT/US98/04482 Non-provisional of 60/047,598 May 23, 1997 PCT/US98/04482 Non-provisional of 60/047,613 May 23, 1997 PCT/US98/04482 Non-provisional of 60/047,582 May 23, 1997 PCT/US98/04482 Non-provisional of 60/047,596 May 23, 1997 PCT/US98/04482 Non-provisional of 60/047,612 May 23, 1997 PCT/US98/04482 Non-provisional of 60/047,632 May 23, 1997 PCT/US98/04482 Non-provisional of 60/047,601 May 23, 1997 PCT/US98/04482 Non-provisional of 60/043,580 Apr. 11, 1997 PCT/US98/04482 Non-provisional of 60/043,568 Apr. 11, 1997 PCT/US98/04482 Non-provisional of 60/043,314 Apr. 11, 1997 PCT/US98/04482 Non-provisional of 60/043,569 Apr. 11, 1997 PCT/US98/04482 Non-provisional of 60/043,311 Apr. 11, 1997 PCT/US98/04482 Non-provisional of 60/043,671 Apr. 11, 1997 PCT/US98/04482 Non-provisional of 60/043,674 Apr. 11, 1997 PCT/US98/04482 Non-provisional of 60/043,669 Apr. 11, 1997 PCT/US98/04482 Non-provisional of 60/043,312 Apr. 11, 1997 PCT/US98/04482 Non-provisional of 60/043,313 Apr. 11, 1997 PCT/US98/04482 Non-provisional of 60/043,672 Apr. 11, 1997 PCT/US98/04482 Non-provisional of 60/043,315 Apr. 11, 1997 PCT/US98/04482 Non-provisional of 60/048,974 Jun. 06, 1997 PCT/US98/04482 Non-provisional of 60/056,886 Aug. 22, 1997 PCT/US98/04482 Non-provisional of 60/056,877 Aug. 22, 1997 PCT/US98/04482 Non-provisional of 60/056,889 Aug. 22, 1997 PCT/US98/04482 Non-provisional of 60/056,893 Aug. 22, 1997 PCT/US98/04482 Non-provisional of 60/056,630 Aug. 22, 1997 PCT/US98/04482 Non-provisional of 60/056,878 Aug. 22, 1997 PCT/US98/04482 Non-provisional of 60/056,662 Aug. 22, 1997 PCT/US98/04482 Non-provisional of 60/056,872 Aug. 22, 1997 PCT/US98/04482 Non-provisional of 60/056,882 Aug. 22, 1997 PCT/US98/04482 Non-provisional of 60/056,637 Aug. 22, 1997 PCT/US98/04482 Non-provisional of 60/056,903 Aug. 22, 1997 PCT/US98/04482 Non-provisional of 60/056,888 Aug. 22, 1997 PCT/US98/04482 Non-provisional of 60/056,879 Aug. 22, 1997 PCT/US98/04482 Non-provisional of 60/056,880 Aug. 22, 1997 PCT/US98/04482 Non-provisional of 60/056,894 Aug. 22, 1997 PCT/US98/04482 Non-provisional of 60/056,911 Aug. 22, 1997 PCT/US98/04482 Non-provisional of 60/056,636 Aug. 22, 1997 PCT/US98/04482 Non-provisional of 60/056,874 Aug. 22, 1997 PCT/US98/04482 Non-provisional of 60/056,910 Aug. 22, 1997 PCT/US98/04482 Non-provisional of 60/056,864 Aug. 22, 1997 PCT/US98/04482 Non-provisional of 60/056,631 Aug. 22, 1997 PCT/US98/04482 Non-provisional of 60/056,845 Aug. 22, 1997 PCT/US98/04482 Non-provisional of 60/056,892 Aug. 22, 1997 PCT/US98/04482 Non-provisional of 60/047,595 May 23, 1997 PCT/US98/04482 Non-provisional of 60/057,761 Sep. 05, 1997 PCT/US98/04482 Non-provisional of 60/047,599 May 23, 1997 PCT/US98/04482 Non-provisional of 60/047,588 May 23, 1997 PCT/US98/04482 Non-provisional of 60/047,585 May 23, 1997 PCT/US98/04482 Non-provisional of 60/047,586 May 23, 1997 PCT/US98/04482 Non-provisional of 60/047,590 May 23, 1997 PCT/US98/04482 Non-provisional of 60/047,594 May 23, 1997 PCT/US98/04482 Non-provisional of 60/047,589 May 23, 1997 PCT/US98/04482 Non-provisional of 60/047,593 May 23, 1997 PCT/US98/04482 Non-provisional of 60/047,614 May 23, 1997 PCT/US98/04482 Non-provisional of 60/043,578 Apr. 11, 1997 PCT/US98/04482 Non-provisional of 60/043,576 Apr. 11, 1997 PCT/US98/04482 Non-provisional of 60/047,501 May 23, 1997 PCT/US98/04482 Non-provisional of 60/043,670 Apr. 11, 1997 PCT/US98/04482 Non-provisional of 60/056,632 Aug. 22, 1997 PCT/US98/04482 Non-provisional of 60/056,664 Aug. 22, 1997 PCT/US98/04482 Non-provisional of 60/056,876 Aug. 22, 1997 PCT/US98/04482 Non-provisional of 60/056,881 Aug. 22, 1997 PCT/US98/04482 Non-provisional of 60/056,909 Aug. 22, 1997 PCT/US98/04482 Non-provisional of 60/056,875 Aug. 22, 1997 PCT/US98/04482 Non-provisional of 60/056,862 Aug. 22, 1997 PCT/US98/04482 Non-provisional of 60/056,887 Aug. 22, 1997 PCT/US98/04482 Non-provisional of 60/056,908 Aug. 22, 1997 PCT/US98/04482 Non-provisional of 60/048,964 Jun. 06, 1997 PCT/US98/04482 Non-provisional of 60/057,650 Sep. 05, 1997 PCT/US98/04482 Non-provisional of 60/056,884 Aug. 22, 1997 10/100,683 Continuation-in-part of 09/882,171 Jun. 18, 2001 09/882,171 Non-provisional of 60/190,068 Mar. 17, 2000 09/882,171 Continuation of 09/809,391 Mar. 16, 2001 09/809,391 Continuation-in-part of 09/149,476 Sep. 08, 1998 09/149,476 Continuation-in-part of PCT/US98/04493 Mar. 06, 1998 10/100,683 Continuation-in-part of 09/809,391 Mar. 16, 2001 09/809,391 Non-provisional of 60/190,068 Mar. 17, 2000 09/809,391 Continuation-in-part of 09/149,476 Sep. 08, 1998 09/149,476 Continuation-in-part of PCT/US98/04493 Mar. 06, 1998 10/100,683 Continuation-in-part of 09/149,476 Sep. 08, 1998 09/149,476 Continuation-in-part of PCT/US98/04493 Mar. 06, 1998 10/100,683 Continuation-in-part of PCT/US98/04493 Mar. 06, 1998 PCT/US98/04493 Non-provisional of 60/040,161 Mar. 07, 1997 PCT/US98/04493 Non-provisional of 60/040,162 Mar. 07, 1997 PCT/US98/04493 Non-provisional of 60/040,333 Mar. 07, 1997 PCT/US98/04493 Non-provisional of 60/038,621 Mar. 07, 1997 PCT/US98/04493 Non-provisional of 60/040,626 Mar. 07, 1997 PCT/US98/04493 Non-provisional of 60/040,334 Mar. 07, 1997 PCT/US98/04493 Non-provisional of 60/040,336 Mar. 07, 1997 PCT/US98/04493 Non-provisional of 60/040,163 Mar. 07, 1997 PCT/US98/04493 Non-provisional of 60/047,600 May 23, 1997 PCT/US98/04493 Non-provisional of 60/047,615 May 23, 1997 PCT/US98/04493 Non-provisional of 60/047,597 May 23, 1997 PCT/US98/04493 Non-provisional of 60/047,502 May 23, 1997 PCT/US98/04493 Non-provisional of 60/047,633 May 23, 1997 PCT/US98/04493 Non-provisional of 60/047,583 May 23, 1997 PCT/US98/04493 Non-provisional of 60/047,617 May 23, 1997 PCT/US98/04493 Non-provisional of 60/047,618 May 23, 1997 PCT/US98/04493 Non-provisional of 60/047,503 May 23, 1997 PCT/US98/04493 Non-provisional of 60/047,592 May 23, 1997 PCT/US98/04493 Non-provisional of 60/047,581 May 23, 1997 PCT/US98/04493 Non-provisional of 60/047,584 May 23, 1997 PCT/US98/04493 Non-provisional of 60/047,500 May 23, 1997 PCT/US98/04493 Non-provisional of 60/047,587 May 23, 1997 PCT/US98/04493 Non-provisional of 60/047,492 May 23, 1997 PCT/US98/04493 Non-provisional of 60/047,598 May 23, 1997 PCT/US98/04493 Non-provisional of 60/047,613 May 23, 1997 PCT/US98/04493 Non-provisional of 60/047,582 May 23, 1997 PCT/US98/04493 Non-provisional of 60/047,596 May 23, 1997 PCT/US98/04493 Non-provisional of 60/047,612 May 23, 1997 PCT/US98/04493 Non-provisional of 60/047,632 May 23, 1997 PCT/US98/04493 Non-provisional of 60/047,601 May 23, 1997 PCT/US98/04493 Non-provisional of 60/043,580 Apr. 11, 1997 PCT/US98/04493 Non-provisional of 60/043,568 Apr. 11, 1997 PCT/US98/04493 Non-provisional of 60/043,314 Apr. 11, 1997 PCT/US98/04493 Non-provisional of 60/043,569 Apr. 11, 1997 PCT/US98/04493 Non-provisional of 60/043,311 Apr. 11, 1997 PCT/US98/04493 Non-provisional of 60/043,671 Apr. 11, 1997 PCT/US98/04493 Non-provisional of 60/043,674 Apr. 11, 1997 PCT/US98/04493 Non-provisional of 60/043,669 Apr. 11, 1997 PCT/US98/04493 Non-provisional of 60/043,312 Apr. 11, 1997 PCT/US98/04493 Non-provisional of 60/043,313 Apr. 11, 1997 PCT/US98/04493 Non-provisional of 60/043,672 Apr. 11, 1997 PCT/US98/04493 Non-provisional of 60/043,315 Apr. 11, 1997 PCT/US98/04493 Non-provisional of 60/048,974 Jun. 06, 1997 PCT/US98/04493 Non-provisional of 60/056,886 Aug. 22, 1997 PCT/US98/04493 Non-provisional of 60/056,877 Aug. 22, 1997 PCT/US98/04493 Non-provisional of 60/056,889 Aug. 22, 1997 PCT/US98/04493 Non-provisional of 60/056,893 Aug. 22, 1997 PCT/US98/04493 Non-provisional of 60/056,630 Aug. 22, 1997 PCT/US98/04493 Non-provisional of 60/056,878 Aug. 22, 1997 PCT/US98/04493 Non-provisional of 60/056,662 Aug. 22, 1997 PCT/US98/04493 Non-provisional of 60/056,872 Aug. 22, 1997 PCT/US98/04493 Non-provisional of 60/056,882 Aug. 22, 1997 PCT/US98/04493 Non-provisional of 60/056,637 Aug. 22, 1997 PCT/US98/04493 Non-provisional of 60/056,903 Aug. 22, 1997 PCT/US98/04493 Non-provisional of 60/056,888 Aug. 22, 1997 PCT/US98/04493 Non-provisional of 60/056,879 Aug. 22, 1997 PCT/US98/04493 Non-provisional of 60/056,880 Aug. 22, 1997 PCT/US98/04493 Non-provisional of 60/056,894 Aug. 22, 1997 PCT/US98/04493 Non-provisional of 60/056,911 Aug. 22, 1997 PCT/US98/04493 Non-provisional of 60/056,636 Aug. 22, 1997 PCT/US98/04493 Non-provisional of 60/056,874 Aug. 22, 1997 PCT/US98/04493 Non-provisional of 60/056,910 Aug. 22, 1997 PCT/US98/04493 Non-provisional of 60/056,864 Aug. 22, 1997 PCT/US98/04493 Non-provisional of 60/056,631 Aug. 22, 1997 PCT/US98/04493 Non-provisional of 60/056,845 Aug. 22, 1997 PCT/US98/04493 Non-provisional of 60/056,892 Aug. 22, 1997 PCT/US98/04493 Non-provisional of 60/057,761 Sep. 05, 1997 PCT/US98/04493 Non-provisional of 60/047,595 May 23, 1997 PCT/US98/04493 Non-provisional of 60/047,599 May 23, 1997 PCT/US98/04493 Non-provisional of 60/047,588 May 23, 1997 PCT/US98/04493 Non-provisional of 60/047,585 May 23, 1997 PCT/US98/04493 Non-provisional of 60/047,586 May 23, 1997 PCT/US98/04493 Non-provisional of 60/047,590 May 23, 1997 PCT/US98/04493 Non-provisional of 60/047,594 May 23, 1997 PCT/US98/04493 Non-provisional of 60/047,589 May 23, 1997 PCT/US98/04493 Non-provisional of 60/047,593 May 23, 1997 PCT/US98/04493 Non-provisional of 60/047,614 May 23, 1997 PCT/US98/04493 Non-provisional of 60/043,578 Apr. 11, 1997 PCT/US98/04493 Non-provisional of 60/043,576 Apr. 11, 1997 PCT/US98/04493 Non-provisional of 60/047,501 May 23, 1997 PCT/US98/04493 Non-provisional of 60/043,670 Apr. 11, 1997 PCT/US98/04493 Non-provisional of 60/056,632 Aug. 22, 1997 PCT/US98/04493 Non-provisional of 60/056,664 Aug. 22, 1997 PCT/US98/04493 Non-provisional of 60/056,876 Aug. 22, 1997 PCT/US98/04493 Non-provisional of 60/056,881 Aug. 22, 1997 PCT/US98/04493 Non-provisional of 60/056,909 Aug. 22, 1997 PCT/US98/04493 Non-provisional of 60/056,875 Aug. 22, 1997 PCT/US98/04493 Non-provisional of 60/056,862 Aug. 22, 1997 PCT/US98/04493 Non-provisional of 60/056,887 Aug. 22, 1997 PCT/US98/04493 Non-provisional of 60/056,908 Aug. 22, 1997 PCT/US98/04493 Non-provisional of 60/048,964 Jun. 06, 1997 PCT/US98/04493 Non-provisional of 60/057,650 Sep. 05, 1997 PCT/US98/04493 Non-provisional of 60/056,884 Aug. 22, 1997 PCT/US98/04493 Non-provisional of 60/057,669 Sep. 05, 1997 PCT/US98/04493 Non-provisional of 60/049,610 Jun. 13, 1997 PCT/US98/04493 Non-provisional of 60/061,060 Oct. 02, 1997 PCT/US98/04493 Non-provisional of 60/051,926 Jul. 08, 1997 PCT/US98/04493 Non-provisional of 60/052,874 Jul. 16, 1997 PCT/US98/04493 Non-provisional of 60/058,785 Sep. 12, 1997 PCT/US98/04493 Non-provisional of 60/055,724 Aug. 18, 1997 10/100,683 Continuation-in-part of 10/058,993 Jan. 30, 2002 10/058,993 Non-provisional of 60/265,583 Feb. 02, 2001 10/058,993 Continuation-in-part of 09/852,659 May 11, 2001 09/852,659 Continuation-in-part of 09/152,060 Sep. 11, 1998 09/152,060 Continuation-in-part of PCT/US98/04858 Mar. 12, 1998 10/058,993 Continuation-in-part of 09/853,161 May 11, 2001 09/853,161 Continuation-in-part of 09/152,060 Sep. 11, 1998 09/152,060 Continuation-in-part of PCT/US98/04858 Mar. 12, 1998 10/058,993 Continuation-in-part of 09/852,797 May 11, 2001 09/852,797 Continuation-in-part of 09/152,060 Sep. 11, 1998 09/152,060 Continuation-in-part of PCT/US98/04858 Mar. 12, 1998 10/100,683 Continuation-in-part of 09/852,659 May 11, 2001 09/852,659 Non-provisional of 60/265,583 Feb. 02, 2001 09/852,659 Continuation-in-part of 09/152,060 Sep. 11, 1998 09/152,060 Continuation-in-part of PCT/US98/04858 Mar. 12, 1998 10/100,683 Continuation-in-part of 09/853,161 May 11, 2001 09/853,161 Non-provisional of 60/265,583 Feb. 02, 2001 09/853,161 Continuation-in-part of 09/152,060 Sep. 11, 1998 09/152,060 Continuation-in-part of PCT/US98/04858 Mar. 12, 1998 10/100,683 Continuation-in-part of 09/852,797 May 11, 2001 09/852,797 Non-provisional of 60/265,583 Feb. 02, 2001 09/852,797 Continuation-in-part of 09/152,060 Sep. 11, 1998 09/152,060 Continuation-in-part of PCT/US98/04858 Mar. 12, 1998 10/100,683 Continuation-in-part of 09/152,060 Sep. 11, 1998 09/152,060 Continuation-in-part of PCT/US98/04858 Mar. 12, 1998 10/100,683 Continuation-in-part of PCT/US98/04858 Mar. 12, 1998 PCT/US98/04858 Non-provisional of 60/040,762 Mar. 14, 1997 PCT/US98/04858 Non-provisional of 60/040,710 Mar. 14, 1997 PCT/US98/04858 Non-provisional of 60/050,934 May 30, 1997 PCT/US98/04858 Non-provisional of 60/048,100 May 30, 1997 PCT/US98/04858 Non-provisional of 60/048,357 May 30, 1997 PCT/US98/04858 Non-provisional of 60/048,189 May 30, 1997 PCT/US98/04858 Non-provisional of 60/057,765 Sep. 05, 1997 PCT/US98/04858 Non-provisional of 60/048,970 Jun. 06, 1997 PCT/US98/04858 Non-provisional of 60/068,368 Dec. 19, 1997 10/100,683 Continuation-in-part of 10/059,395 Jan. 31, 2002 10/059,395 Divisional of 09/966,262 Oct. 01, 2001 09/966,262 Continuation of 09/154,707 Sep. 17, 1998 09/154,707 Continuation-in-part of PCT/US98/05311 Mar. 19, 1998 10/100,683 Continuation-in-part of 09/984,245 Oct. 29, 2001 09/984,245 Divisional of 09/154,707 Sep. 17, 1998 09/154,707 Continuation-in-part of PCT/US98/05311 Mar. 19, 1998 10/100,683 Continuation-in-part of 09/983,966 Oct. 26, 2001 09/983,966 Divisional of 09/154,707 Sep. 17, 1998 09/154,707 Continuation-in-part of PCT/US98/05311 Mar. 19, 1998 10/100,683 Continuation-in-part of 09/966,262 Oct. 01, 2001 09/966,262 Continuation of of 09/154,707 Sep. 17, 1998 09/154,707 Continuation-in-part of PCT/US98/05311 Mar. 19, 1998 10/100,683 Continuation-in-part of 09/154,707 Sep. 17, 1998 09/154,707 Continuation-in-part of PCT/US98/05311 Mar. 19, 1998 10/100,683 Continuation-in-part of PCT/US98/05311 Mar. 03, 1998 PCT/US98/05311 Non-provisional of 60/041,277 Mar. 21, 1997 PCT/US98/05311 Non-provisional of 60/042,344 Mar. 21, 1997 PCT/US98/05311 Non-provisional of 60/041,276 Mar. 21, 1997 PCT/US98/05311 Non-provisional of 60/041,281 Mar. 21, 1997 PCT/US98/05311 Non-provisional of 60/048,094 May 30, 1997 PCT/US98/05311 Non-provisional of 60/048,350 May 30, 1997 PCT/US98/05311 Non-provisional of 60/048,188 May 30, 1997 PCT/US98/05311 Non-provisional of 60/048,135 May 30, 1997 PCT/US98/05311 Non-provisional of 60/050,937 May 30, 1997 PCT/US98/05311 Non-provisional of 60/048,187 May 30, 1997 PCT/US98/05311 Non-provisional of 60/048,099 May 30, 1997 PCT/US98/05311 Non-provisional of 60/048,352 May 30, 1997 PCT/US98/05311 Non-provisional of 60/048,186 May 30, 1997 PCT/US98/05311 Non-provisional of 60/048,069 May 30, 1997 PCT/US98/05311 Non-provisional of 60/048,095 May 30, 1997 PCT/US98/05311 Non-provisional of 60/048,131 May 30, 1997 PCT/US98/05311 Non-provisional of 60/048,096 May 30, 1997 PCT/US98/05311 Non-provisional of 60/048,355 May 30, 1997 PCT/US98/05311 Non-provisional of 60/048,160 May 30, 1997 PCT/US98/05311 Non-provisional of 60/048,351 May 30, 1997 PCT/US98/05311 Non-provisional of 60/048,154 May 30, 1997 PCT/US98/05311 Non-provisional of 60/054,804 Aug. 05, 1997 PCT/US98/05311 Non-provisional of 60/056,370 Aug. 19, 1997 PCT/US98/05311 Non-provisional of 60/060,862 Oct. 02, 1997 10/100,683 Continuation-in-part of 09/814,122 Mar. 22, 2001 09/814,122 Continuation of 09/577,145 May 24, 2000 09/577,145 Continuation of 09/166,780 Oct. 06, 1998 09/166,780 Continuation-in-part of PCT/US98/06801 Apr. 07, 1998 10/100,683 Continuation-in-part of PCT/US98/06801 Apr. 07, 1998 PCT/US98/06801 Non-provisional of 60/042,726 Apr. 08, 1997 PCT/US98/06801 Non-provisional of 60/042,727 Apr. 08, 1997 PCT/US98/06801 Non-provisional of 60/042,728 Apr. 08, 1997 PCT/US98/06801 Non-provisional of 60/042,754 Apr. 08, 1997 PCT/US98/06801 Non-provisional of 60/042,825 Apr. 08, 1997 PCT/US98/06801 Non-provisional of 60/048,068 May 30, 1997 PCT/US98/06801 Non-provisional of 60/048,070 May 30, 1997 PCT/US98/06801 Non-provisional of 60/048,184 May 30, 1997 10/100,683 Continuation-in-part of PCT/US98/06801 Apr. 07, 1997 PCT/US98/06801 Non-provisional of 60/042,726 Apr. 08, 1997 PCT/US98/06801 Non-provisional of 60/042,727 Apr. 08, 1997 PCT/US98/06801 Non-provisional of 60/042,728 Apr. 08, 1997 PCT/US98/06801 Non-provisional of 60/042,754 Apr. 08, 1997 PCT/US98/06801 Non-provisional of 60/042,825 Apr. 08, 1997 PCT/US98/06801 Non-provisional of 60/048,068 May 30, 1997 PCT/US98/06801 Non-provisional of 60/048,070 May 30, 1997 PCT/US98/06801 Non-provisional of 60/048,184 May 30, 1997 10/100,683 Continuation-in-part of PCT/US98/10868 May 28, 1998 PCT/US98/10868 Non-provisional of 60/044,039 May 30, 1997 PCT/US98/10868 Non-provisional of 60/048,093 May 30, 1997 PCT/US98/10868 Non-provisional of 60/048,190 May 30, 1997 PCT/US98/10868 Non-provisional of 60/050,935 May 30, 1997 PCT/US98/10868 Non-provisional of 60/048,101 May 30, 1997 PCT/US98/10868 Non-provisional of 60/048,356 May 30, 1997 PCT/US98/10868 Non-provisional of 60/056,250 Aug. 29, 1997 PCT/US98/10868 Non-provisional of 60/056,296 Aug. 29, 1997 PCT/US98/10868 Non-provisional of 60/056,293 Aug. 29, 1997 10/100,683 Continuation-in-part of PCT/US98/11422 Jun. 04, 1998 PCT/US98/11422 Non-provisional of 60/048,885 Jun. 06, 1997 PCT/US98/11422 Non-provisional of 60/049,375 Jun. 06, 1997 PCT/US98/11422 Non-provisional of 60/048,881 Jun. 06, 1997 PCT/US98/11422 Non-provisional of 60/048,880 Jun. 06, 1997 PCT/US98/11422 Non-provisional of 60/048,896 Jun. 06, 1997 PCT/US98/11422 Non-provisional of 60/049,020 Jun. 06, 1997 PCT/US98/11422 Non-provisional of 60/048,876 Jun. 06, 1997 PCT/US98/11422 Non-provisional of 60/048,895 Jun. 06, 1997 PCT/US98/11422 Non-provisional of 60/048,884 Jun. 06, 1997 PCT/US98/11422 Non-provisional of 60/048,894 Jun. 06, 1997 PCT/US98/11422 Non-provisional of 60/048,971 Jun. 06, 1997 PCT/US98/11422 Non-provisional of 60/048,964 Jun. 06, 1997 PCT/US98/11422 Non-provisional of 60/048,882 Jun. 06, 1997 PCT/US98/11422 Non-provisional of 60/048,899 Jun. 06, 1997 PCT/US98/11422 Non-provisional of 60/048,893 Jun. 06, 1997 PCT/US98/11422 Non-provisional of 60/048,900 Jun. 06, 1997 PCT/US98/11422 Non-provisional of 60/048,901 Jun. 06, 1997 PCT/US98/11422 Non-provisional of 60/048,892 Jun. 06, 1997 PCT/US98/11422 Non-provisional of 60/048,915 Jun. 06, 1997 PCT/US98/11422 Non-provisional of 60/049,019 Jun. 06, 1997 PCT/US98/11422 Non-provisional of 60/048,970 Jun. 06, 1997 PCT/US98/11422 Non-provisional of 60/048,972 Jun. 06, 1997 PCT/US98/11422 Non-provisional of 60/048,916 Jun. 06, 1997 PCT/US98/11422 Non-provisional of 60/049,373 Jun. 06, 1997 PCT/US98/11422 Non-provisional of 60/048,875 Jun. 06, 1997 PCT/US98/11422 Non-provisional of 60/049,374 Jun. 06, 1997 PCT/US98/11422 Non-provisional of 60/048,917 Jun. 06, 1997 PCT/US98/11422 Non-provisional of 60/048,949 Jun. 06, 1997 PCT/US98/11422 Non-provisional of 60/048,974 Jun. 06, 1997 PCT/US98/11422 Non-provisional of 60/048,883 Jun. 06, 1997 PCT/US98/11422 Non-provisional of 60/048,897 Jun. 06, 1997 PCT/US98/11422 Non-provisional of 60/048,898 Jun. 06, 1997 PCT/US98/11422 Non-provisional of 60/048,962 Jun. 06, 1997 PCT/US98/11422 Non-provisional of 60/048,963 Jun. 06, 1997 PCT/US98/11422 Non-provisional of 60/048,877 Jun. 06, 1997 PCT/US98/11422 Non-provisional of 60/048,878 Jun. 06, 1997 PCT/US98/11422 Non-provisional of 60/057,645 Sep. 05, 1997 PCT/US98/11422 Non-provisional of 60/057,642 Sep. 05, 1997 PCT/US98/11422 Non-provisional of 60/057,668 Sep. 05, 1997 PCT/US98/11422 Non-provisional of 60/057,635 Sep. 05, 1997 PCT/US98/11422 Non-provisional of 60/057,627 Sep. 05, 1997 PCT/US98/11422 Non-provisional of 60/057,667 Sep. 05, 1997 PCT/US98/11422 Non-provisional of 60/057,666 Sep. 05, 1997 PCT/US98/11422 Non-provisional of 60/057,764 Sep. 05, 1997 PCT/US98/11422 Non-provisional of 60/057,643 Sep. 05, 1997 PCT/US98/11422 Non-provisional of 60/057,769 Sep. 05, 1997 PCT/US98/11422 Non-provisional of 60/057,763 Sep. 05, 1997 PCT/US98/11422 Non-provisional of 60/057,650 Sep. 05, 1997 PCT/US98/11422 Non-provisional of 60/057,584 Sep. 05, 1997 PCT/US98/11422 Non-provisional of 60/057,647 Sep. 05, 1997 PCT/US98/11422 Non-provisional of 60/057,661 Sep. 05, 1997 PCT/US98/11422 Non-provisional of 60/057,662 Sep. 05, 1997 PCT/US98/11422 Non-provisional of 60/057,646 Sep. 05, 1997 PCT/US98/11422 Non-provisional of 60/057,654 Sep. 05, 1997 PCT/US98/11422 Non-provisional of 60/057,651 Sep. 05, 1997 PCT/US98/11422 Non-provisional of 60/057,644 Sep. 05, 1997 PCT/US98/11422 Non-provisional of 60/057,765 Sep. 05, 1997 PCT/US98/11422 Non-provisional of 60/057,762 Sep. 05, 1997 PCT/US98/11422 Non-provisional of 60/057,775 Sep. 05, 1997 PCT/US98/11422 Non-provisional of 60/057,648 Sep. 05, 1997 PCT/US98/11422 Non-provisional of 60/057,774 Sep. 05, 1997 PCT/US98/11422 Non-provisional of 60/057,649 Sep. 05, 1997 PCT/US98/11422 Non-provisional of 60/057,770 Sep. 05, 1997 PCT/US98/11422 Non-provisional of 60/057,771 Sep. 05, 1997 PCT/US98/11422 Non-provisional of 60/057,761 Sep. 05, 1997 PCT/US98/11422 Non-provisional of 60/057,760 Sep. 05, 1997 PCT/US98/11422 Non-provisional of 60/057,776 Sep. 05, 1997 PCT/US98/11422 Non-provisional of 60/057,778 Sep. 05, 1997 PCT/US98/11422 Non-provisional of 60/057,629 Sep. 05, 1997 PCT/US98/11422 Non-provisional of 60/057,628 Sep. 05, 1997 PCT/US98/11422 Non-provisional of 60/057,777 Sep. 05, 1997 PCT/US98/11422 Non-provisional of 60/057,634 Sep. 05, 1997 PCT/US98/11422 Non-provisional of 60/070,923 Dec. 18, 1997 10/100,683 Continuation-in-part of PCT/US01/05614 Feb. 21, 2001 PCT/US01/05614 Non-provisional of 60/184,836 Feb. 24, 2000 PCT/US01/05614 Non-provisional of 60/193,170 Mar. 29, 2000 10/100,683 Continuation-in-part of PCT/US98/12125 Jun. 11, 1998 PCT/US98/12125 Non-provisional of 60/049,547 Jun. 13, 1997 PCT/US98/12125 Non-provisional of 60/049,548 Jun. 13, 1997 PCT/US98/12125 Non-provisional of 60/049,549 Jun. 13, 1997 PCT/US98/12125 Non-provisional of 60/049,550 Jun. 13, 1997 PCT/US98/12125 Non-provisional of 60/049,566 Jun. 13, 1997 PCT/US98/12125 Non-provisional of 60/049,606 Jun. 13, 1997 PCT/US98/12125 Non-provisional of 60/049,607 Jun. 13, 1997 PCT/US98/12125 Non-provisional of 60/049,608 Jun. 13, 1997 PCT/US98/12125 Non-provisional of 60/049,609 Jun. 13, 1997 PCT/US98/12125 Non-provisional of 60/049,610 Jun. 13, 1997 PCT/US98/12125 Non-provisional of 60/049,611 Jun. 13, 1997 PCT/US98/12125 Non-provisional of 60/050,901 Jun. 13, 1997 PCT/US98/12125 Non-provisional of 60/052,989 Jun. 13, 1997 PCT/US98/12125 Non-provisional of 60/051,919 Jul. 08, 1997 PCT/US98/12125 Non-provisional of 60/055,984 Aug. 18, 1997 PCT/US98/12125 Non-provisional of 60/058,665 Sep. 12, 1997 PCT/US98/12125 Non-provisional of 60/058,668 Sep. 12, 1997 PCT/US98/12125 Non-provisional of 60/058,669 Sep. 12, 1997 PCT/US98/12125 Non-provisional of 60/058,750 Sep. 12, 1997 PCT/US98/12125 Non-provisional of 60/058,971 Sep. 12, 1997 PCT/US98/12125 Non-provisional of 60/058,972 Sep. 12, 1997 PCT/US98/12125 Non-provisional of 60/058,975 Sep. 12, 1997 PCT/US98/12125 Non-provisional of 60/060,834 Oct. 02, 1997 PCT/US98/12125 Non-provisional of 60/060,841 Oct. 02, 1997 PCT/US98/12125 Non-provisional of 60/060,844 Oct. 02, 1997 PCT/US98/12125 Non-provisional of 60/060,865 Oct. 02, 1997 PCT/US98/12125 Non-provisional of 60/061,059 Oct. 02, 1997 PCT/US98/12125 Non-provisional of 60/061,060 Oct. 02, 1997 10/100,683 Continuation-in-part of 09/627,081 Jul. 27, 2000 09/627,081 Continuation of 09/213,365 Dec. 17, 1998 09/213,365 Continuation-in-part of PCT/US98/13608 Jun. 30, 1998 10/100,683 Continuation-in-part of PCT/US98/13608 Jun. 30, 1998 PCT/US98/13608 Non-provisional of 60/051,480 Jul. 01, 1997 PCT/US98/13608 Non-provisional of 60/051,381 Jul. 01, 1997 PCT/US98/13608 Non-provisional of 60/058,663 Sep. 12, 1997 PCT/US98/13608 Non-provisional of 60/058,598 Sep. 12, 1997 10/100,683 Continuation-in-part of 09/984,490 Oct. 30, 2001 09/984,490 Divisional of 09/227,357 Jan. 08, 1999 09/227,357 Continuation-in-part of PCT/US98/13684 Jul. 07, 1998 10/100,683 Continuation-in-part of 09/983,802 Oct. 25, 2001 09/983,802 Continuation of 09/227,357 Oct. 10, 2001 09/227,357 Continuation-in-part of PCT/US98/13684 Jul. 07, 1998 10/100,683 Continuation-in-part of 09/973,278 Oct. 10, 2001 09/973,278 Non-provisional of 60/239,899 Oct. 13, 2000 09/973,278 Continuation-in-part of 09/227,357 Jan. 08, 1999 09/227,357 Continuation-in-part of PCT/US98/13684 Jul. 07, 1998 10/100,683 Continuation-in-part of PCT/US98/13684 Jul. 07, 1998 PCT/US98/13684 Non-provisional of 60/051,926 Jul. 08, 1997 PCT/US98/13684 Non-provisional of 60/052,793 Jul. 08, 1997 PCT/US98/13684 Non-provisional of 60/051,925 Jul. 08, 1997 PCT/US98/13684 Non-provisional of 60/051,929 Jul. 08, 1997 PCT/US98/13684 Non-provisional of 60/052,803 Jul. 08, 1997 PCT/US98/13684 Non-provisional of 60/052,732 Jul. 08, 1997 PCT/US98/13684 Non-provisional of 60/051,931 Jul. 08, 1997 PCT/US98/13684 Non-provisional of 60/051,932 Jul. 08, 1997 PCT/US98/13684 Non-provisional of 60/051,916 Jul. 08, 1997 PCT/US98/13684 Non-provisional of 60/051,930 Jul. 08, 1997 PCT/US98/13684 Non-provisional of 60/051,918 Jul. 08, 1997 PCT/US98/13684 Non-provisional of 60/051,920 Jul. 08, 1997 PCT/US98/13684 Non-provisional of 60/052,733 Jul. 08, 1997 PCT/US98/13684 Non-provisional of 60/052,795 Jul. 08, 1997 PCT/US98/13684 Non-provisional of 60/051,919 Jul. 08, 1997 PCT/US98/13684 Non-provisional of 60/051,928 Jul. 08, 1997 PCT/US98/13684 Non-provisional of 60/055,722 Aug. 18, 1997 PCT/US98/13684 Non-provisional of 60/055,723 Aug. 18, 1997 PCT/US98/13684 Non-provisional of 60/055,948 Aug. 18, 1997 PCT/US98/13684 Non-provisional of 60/055,949 Aug. 18, 1997 PCT/US98/13684 Non-provisional of 60/055,953 Aug. 18, 1997 PCT/US98/13684 Non-provisional of 60/055,950 Aug. 18, 1997 PCT/US98/13684 Non-provisional of 60/055,947 Aug. 18, 1997 PCT/US98/13684 Non-provisional of 60/055,964 Aug. 18, 1997 PCT/US98/13684 Non-provisional of 60/056,360 Aug. 18, 1997 PCT/US98/13684 Non-provisional of 60/055,684 Aug. 18, 1997 PCT/US98/13684 Non-provisional of 60/055,984 Aug. 18, 1997 PCT/US98/13684 Non-provisional of 60/055,954 Aug. 18, 1997 PCT/US98/13684 Non-provisional of 60/058,785 Sep. 12, 1997 PCT/US98/13684 Non-provisional of 60/058,664 Sep. 12, 1997 PCT/US98/13684 Non-provisional of 60/058,660 Sep. 12, 1997 PCT/US98/13684 Non-provisional of 60/058,661 Sep. 12, 1997 10/100,683 Continuation-in-part of 09/776,724 Feb. 06, 2001 09/776,724 Non-provisional of 60/180,909 Feb. 08, 2000 09/776,724 Continuation-in-part of 09/669,688 Sep. 26, 2000 09/669,688 Continuation of 09/229,982 Jan. 14, 1999 09/229,982 Continuation-in-part of PCT/US98/14613 Jul. 15, 1998 10/100,683 Continuation-in-part of 09/669,688 Sep. 26, 2000 09/669,688 Continuation of 09/229,982 Jan. 14, 1999 09/229,982 Continuation-in-part of PCT/US98/14613 Jul. 15, 1998 10/100,683 Continuation-in-part of 09/229,982 Jan. 14, 1999 09/229,982 Continuation-in-part of PCT/US98/14613 Jul. 15, 1998 10/100,683 Continuation-in-part of PCT/US98/14613 Jul. 15, 1998 PCT/US98/14613 Non-provisional of 60/052,661 Jul. 16, 1997 PCT/US98/14613 Non-provisional of 60/052,872 Jul. 16, 1997 PCT/US98/14613 Non-provisional of 60/052,871 Jul. 16, 1997 PCT/US98/14613 Non-provisional of 60/052,874 Jul. 16, 1997 PCT/US98/14613 Non-provisional of 60/052,873 Jul. 16, 1997 PCT/US98/14613 Non-provisional of 60/052,870 Jul. 16, 1997 PCT/US98/14613 Non-provisional of 60/052,875 Jul. 16, 1997 PCT/US98/14613 Non-provisional of 60/053,440 Jul. 22, 1997 PCT/US98/14613 Non-provisional of 60/053,441 Jul. 22, 1997 PCT/US98/14613 Non-provisional of 60/053,442 Jul. 22, 1997 PCT/US98/14613 Non-provisional of 60/056,359 Aug. 18, 1997 PCT/US98/14613 Non-provisional of 60/055,725 Aug. 18, 1997 PCT/US98/14613 Non-provisional of 60/055,985 Aug. 18, 1997 PCT/US98/14613 Non-provisional of 60/055,952 Aug. 18, 1997 PCT/US98/14613 Non-provisional of 60/055,989 Aug. 18, 1997 PCT/US98/14613 Non-provisional of 60/056,361 Aug. 18, 1997 PCT/US98/14613 Non-provisional of 60/055,726 Aug. 18, 1997 PCT/US98/14613 Non-provisional of 60/055,724 Aug. 18, 1997 PCT/US98/14613 Non-provisional of 60/055,946 Aug. 18, 1997 PCT/US98/14613 Non-provisional of 60/055,683 Aug. 18, 1997 10/100,683 Non-provisional of 60/295,558 Jun. 05, 2001 10/100,683 Continuation-in-part of 09/820,649 Mar. 30, 2001 09/820,649 Continuation of 09/666,984 Sep. 21, 2000 09/666,984 Continuation of 09/236,557 Jan. 26, 1999 09/236,557 Continuation-in-part of PCT/US98/15949 Jul. 29, 1998 10/100,683 Continuation-in-part of PCT/US98/15949 Jul. 29, 1998 PCT/US98/15949 Non-provisional of 60/054,212 Jul. 30, 1997 PCT/US98/15949 Non-provisional of 60/054,209 Jul. 30, 1997 PCT/US98/15949 Non-provisional of 60/054,234 Jul. 30, 1997 PCT/US98/15949 Non-provisional of 60/054,218 Jul. 30, 1997 PCT/US98/15949 Non-provisional of 60/054,214 Jul. 30, 1997 PCT/US98/15949 Non-provisional of 60/054,236 Jul. 30, 1997 PCT/US98/15949 Non-provisional of 60/054,215 Jul. 30, 1997 PCT/US98/15949 Non-provisional of 60/054,211 Jul. 30, 1997 PCT/US98/15949 Non-provisional of 60/054,217 Jul. 30, 1997 PCT/US98/15949 Non-provisional of 60/054,213 Jul. 30, 1997 PCT/US98/15949 Non-provisional of 60/055,968 Aug. 18, 1997 PCT/US98/15949 Non-provisional of 60/055,969 Aug. 18, 1997 PCT/US98/15949 Non-provisional of 60/055,972 Aug. 18, 1997 PCT/US98/15949 Non-provisional of 60/056,561 Aug. 19, 1997 PCT/US98/15949 Non-provisional of 60/056,534 Aug. 19, 1997 PCT/US98/15949 Non-provisional of 60/056,729 Aug. 19, 1997 PCT/US98/15949 Non-provisional of 60/056,543 Aug. 19, 1997 PCT/US98/15949 Non-provisional of 60/056,727 Aug. 19, 1997 PCT/US98/15949 Non-provisional of 60/056,554 Aug. 19, 1997 PCT/US98/15949 Non-provisional of 60/056,730 Aug. 19, 1997 10/100,683 Continuation-in-part of 09/969,730 Oct. 04, 2001 09/969,730 Continuation-in-part of 09/774,639 Feb. 01, 2001 09/774,639 Continuation of 09/244,112 Feb. 04, 1999 09/244,112 Continuation-in-part of PCT/US98/16235 Aug. 04, 1998 10/100,683 Continuation-in-part of 09/774,639 Feb. 01, 2001 09/774,639 Continuation of 09/244,112 Feb. 04, 1999 09/244,112 Continuation-in-part of PCT/US98/16235 Aug. 04, 1998 10/100,683 Continuation-in-part of 09/969,730 Oct. 04, 2001 09/969,730 Non-provisional of 60/238,291 Oct. 06, 2000 10/100,683 Continuation-in-part of PCT/US98/16235 Aug. 04, 1998 PCT/US98/16235 Non-provisional of 60/055,386 Aug. 05, 1997 PCT/US98/16235 Non-provisional of 60/054,807 Aug. 05, 1997 PCT/US98/16235 Non-provisional of 60/055,312 Aug. 05, 1997 PCT/US98/16235 Non-provisional of 60/055,309 Aug. 05, 1997 PCT/US98/16235 Non-provisional of 60/054,798 Aug. 05, 1997 PCT/US98/16235 Non-provisional of 60/055,310 Aug. 05, 1997 PCT/US98/16235 Non-provisional of 60/054,806 Aug. 05, 1997 PCT/US98/16235 Non-provisional of 60/054,809 Aug. 05, 1997 PCT/US98/16235 Non-provisional of 60/054,804 Aug. 05, 1997 PCT/US98/16235 Non-provisional of 60/054,803 Aug. 05, 1997 PCT/US98/16235 Non-provisional of 60/054,808 Aug. 05, 1997 PCT/US98/16235 Non-provisional of 60/055,311 Aug. 05, 1997 PCT/US98/16235 Non-provisional of 60/055,986 Aug. 18, 1997 PCT/US98/16235 Non-provisional of 60/055,970 Aug. 18, 1997 PCT/US98/16235 Non-provisional of 60/056,563 Aug. 19, 1997 PCT/US98/16235 Non-provisional of 60/056,557 Aug. 19, 1997 PCT/US98/16235 Non-provisional of 60/056,731 Aug. 19, 1997 PCT/US98/16235 Non-provisional of 60/056,365 Aug. 19, 1997 PCT/US98/16235 Non-provisional of 60/056,367 Aug. 19, 1997 PCT/US98/16235 Non-provisional of 60/056,370 Aug. 19, 1997 PCT/US98/16235 Non-provisional of 60/056,364 Aug. 19, 1997 PCT/US98/16235 Non-provisional of 60/056,366 Aug. 19, 1997 PCT/US98/16235 Non-provisional of 60/056,732 Aug. 19, 1997 PCT/US98/16235 Non-provisional of 60/056,371 Aug. 19, 1997 10/100,683 Continuation-in-part of 09/716,128 Nov. 17, 2000 09/716,128 Continuation of 09/251,329 Feb. 17, 1999 09/251,329 Continuation-in-part of PCT/US98/17044 Aug. 18, 1998 10/100,683 Continuation-in-part of PCT/US98/17044 Aug. 18, 1998 PCT/US98/17044 Non-provisional of 60/056,555 Aug. 19, 1997 PCT/US98/17044 Non-provisional of 60/056,556 Aug. 19, 1997 PCT/US98/17044 Non-provisional of 60/056,535 Aug. 19, 1997 PCT/US98/17044 Non-provisional of 60/056,629 Aug. 19, 1997 PCT/US98/17044 Non-provisional of 60/056,369 Aug. 19, 1997 PCT/US98/17044 Non-provisional of 60/056,628 Aug. 19, 1997 PCT/US98/17044 Non-provisional of 60/056,728 Aug. 19, 1997 PCT/US98/17044 Non-provisional of 60/056,368 Aug. 19, 1997 PCT/US98/17044 Non-provisional of 60/056,726 Aug. 19, 1997 PCT/US98/17044 Non-provisional of 60/089,510 Jun. 16, 1998 PCT/US98/17044 Non-provisional of 60/092,956 Jul. 15, 1998 10/100,683 Continuation-in-part of 09/729,835 Dec. 06, 2000 09/729,835 Divisional of 09/257,179 Feb. 25, 1999 09/257,179 Continuation-in-part of PCT/US98/17709 Aug. 27, 1998 10/100,683 Continuation-in-part of 09/257,179 Feb. 25, 1999 09/257,179 Continuation-in-part of PCT/US98/17709 Aug. 27, 1998 10/100,683 Continuation-in-part of PCT/US98/17709 Aug. 27, 1998 PCT/US98/17709 Non-provisional of 60/056,270 Aug. 29, 1997 PCT/US98/17709 Non-provisional of 60/056,271 Aug. 29, 1997 PCT/US98/17709 Non-provisional of 60/056,247 Aug. 29, 1997 PCT/US98/17709 Non-provisional of 60/056,073 Aug. 29, 1997 10/100,683 Continuation-in-part of 10/047,021 Jan. 17, 2002 10/047,021 Continuation-in-part of 09/722,329 Nov. 28, 2000 09/722,329 Continuation of 09/262,109 Mar. 04, 1999 09/262,109 Continuation-in-part of PCT/US98/18360 Sep. 03, 1998 10/100,683 Continuation-in-part of 09/722,329 Nov. 28, 2000 09/722,329 Continuation of 09/262,109 Mar. 04, 1999 09/262,109 Continuation-in-part of PCT/US98/18360 Sep. 03, 1998 10/100,683 Continuation-in-part of PZ016pct2 Jan. 17, 2002 PZ016pct2 Non-provisional of 60/262,066 Jan. 18, 2001 10/100,683 Continuation-in-part of PCT/US98/18360 Sep. 03, 1998 PCT/US98/18360 Non-provisional of 60/057,626 Sep. 05, 1997 PCT/US98/18360 Non-provisional of 60/057,663 Sep. 05, 1997 PCT/US98/18360 Non-provisional of 60/057,669 Sep. 05, 1997 PCT/US98/18360 Non-provisional of 60/058,667 Sep. 12, 1997 PCT/US98/18360 Non-provisional of 60/058,974 Sep. 12, 1997 PCT/US98/18360 Non-provisional of 60/058,973 Sep. 12, 1997 PCT/US98/18360 Non-provisional of 60/058,666 Sep. 12, 1997 PCT/US98/18360 Non-provisional of 60/090,112 Jun. 22, 1998 10/100,683 Continuation-in-part of 09/281,976 Mar. 31, 1999 09/281,976 Continuation-in-part of PCT/US98/20775 Oct. 01, 1998 10/100,683 Continuation-in-part of PCT/US98/20775 Oct. 01, 1998 PCT/US98/20775 Non-provisional of 60/060,837 Oct. 02, 1997 PCT/US98/20775 Non-provisional of 60/060,862 Oct. 02, 1997 PCT/US98/20775 Non-provisional of 60/060,839 Oct. 02, 1997 PCT/US98/20775 Non-provisional of 60/060,866 Oct. 02, 1997 PCT/US98/20775 Non-provisional of 60/060,843 Oct. 02, 1997 PCT/US98/20775 Non-provisional of 60/060,836 Oct. 02, 1997 PCT/US98/20775 Non-provisional of 60/060,838 Oct. 02, 1997 PCT/US98/20775 Non-provisional of 60/060,874 Oct. 02, 1997 PCT/US98/20775 Non-provisional of 60/060,833 Oct. 02, 1997 PCT/US98/20775 Non-provisional of 60/060,884 Oct. 02, 1997 PCT/US98/20775 Non-provisional of 60/060,880 Oct. 02, 1997 10/100,683 Continuation-in-part of 09/984,429 Oct. 30, 2001 09/984,429 Non-provisional of 60/244,591 Nov. 01, 2000 09/984,429 Continuation-in-part of 09/288,143 Apr. 08, 1999 09/288,143 Continuation-in-part of PCT/US98/21142 Oct. 08, 1998 10/100,683 Non-provisional of 60/244,591 Nov. 01, 2000 10/100,683 Continuation-in-part of 09/288,143 Apr. 08, 1999 09/288,143 Continuation-in-part of PCT/US98/21142 Oct. 08, 1998 10/100,683 Continuation-in-part of PCT/US98/21142 Oct. 08, 1998 PCT/US98/21142 Non-provisional of 60/061,463 Oct. 09, 1997 PCT/US98/21142 Non-provisional of 60/061,529 Oct. 09, 1997 PCT/US98/21142 Non-provisional of 60/071,498 Oct. 09, 1997 PCT/US98/21142 Non-provisional of 60/061,527 Oct. 09, 1997 PCT/US98/21142 Non-provisional of 60/061,536 Oct. 09, 1997 PCT/US98/21142 Non-provisional of 60/061,532 Oct. 09, 1997 10/100,683 Continuation-in-part of 09/296,622 Apr. 23, 1999 09/296,622 Continuation-in-part of PCT/US98/22376 Oct. 23, 1998 10/100,683 Continuation-in-part of PCT/US98/22376 Oct. 23, 1998 PCT/US98/22376 Non-provisional of 60/063,099 Oct. 24, 1997 PCT/US98/22376 Non-provisional of 60/063,088 Oct. 24, 1997 PCT/US98/22376 Non-provisional of 60/063,100 Oct. 24, 1997 PCT/US98/22376 Non-provisional of 60/063,387 Oct. 24, 1997 PCT/US98/22376 Non-provisional of 60/063,148 Oct. 24, 1997 PCT/US98/22376 Non-provisional of 60/063,386 Oct. 24, 1997 PCT/US98/22376 Non-provisional of 60/062,784 Oct. 24, 1997 PCT/US98/22376 Non-provisional of 60/063,091 Oct. 24, 1997 PCT/US98/22376 Non-provisional of 60/063,090 Oct. 24, 1997 PCT/US98/22376 Non-provisional of 60/063,089 Oct. 24, 1997 PCT/US98/22376 Non-provisional of 60/063,092 Oct. 24, 1997 PCT/US98/22376 Non-provisional of 60/063,111 Oct. 24, 1997 PCT/US98/22376 Non-provisional of 60/063,101 Oct. 24, 1997 PCT/US98/22376 Non-provisional of 60/063,109 Oct. 24, 1997 PCT/US98/22376 Non-provisional of 60/063,110 Oct. 24, 1997 PCT/US98/22376 Non-provisional of 60/063,098 Oct. 24, 1997 PCT/US98/22376 Non-provisional of 60/063,097 Oct. 24, 1997 10/100,683 Continuation-in-part of 09/974,879 Oct. 12, 2001 09/974,879 Non-provisional of 60/239,893 Oct. 13, 2000 09/974,879 Continuation-in-part of 09/818,683 Mar. 28, 2001 09/818,683 Continuation of 09/305,736 May 05, 1999 09/305,736 Continuation-in-part of PCT/US98/23435 Nov. 04, 1998 10/100,683 Continuation-in-part of 09/818,683 Mar. 28, 2001 09/818,683 Continuation of 09/305,736 May 05, 1999 09/305,736 Continuation-in-part of PCT/US98/23435 Nov. 04, 1998 10/100,683 Continuation-in-part of 09/305,736 May 05, 1999 09/305,736 Continuation-in-part of PCT/US98/23435 Nov. 04, 1998 10/100,683 Continuation-in-part of PCT/US98/23435 Nov. 04, 1998 PCT/US98/23435 Non-provisional of 60/064,911 Nov. 07, 1997 PCT/US98/23435 Non-provisional of 60/064,912 Nov. 07, 1997 PCT/US98/23435 Non-provisional of 60/064,983 Nov. 07, 1997 PCT/US98/23435 Non-provisional of 60/064,900 Nov. 07, 1997 PCT/US98/23435 Non-provisional of 60/064,988 Nov. 07, 1997 PCT/US98/23435 Non-provisional of 60/064,987 Nov. 07, 1997 PCT/US98/23435 Non-provisional of 60/064,908 Nov. 07, 1997 PCT/US98/23435 Non-provisional of 60/064,984 Nov. 07, 1997 PCT/US98/23435 Non-provisional of 60/064,985 Nov. 07, 1997 PCT/US98/23435 Non-provisional of 60/066,094 Nov. 17, 1997 PCT/US98/23435 Non-provisional of 60/066,100 Nov. 17, 1997 PCT/US98/23435 Non-provisional of 60/066,089 Nov. 17, 1997 PCT/US98/23435 Non-provisional of 60/066,095 Nov. 17, 1997 PCT/US98/23435 Non-provisional of 60/066,090 Nov. 17, 1997 10/100,683 Continuation-in-part of 09/334,595 Jun. 17, 1999 09/334,595 Continuation-in-part of PCT/US98/27059 Dec. 17, 1998 10/100,683 Continuation-in-part of PCT/US98/27059 Dec. 17, 1998 PCT/US98/27059 Non-provisional of 60/070,923 Dec. 18, 1997 PCT/US98/27059 Non-provisional of 60/068,007 Dec. 18, 1997 PCT/US98/27059 Non-provisional of 60/068,057 Dec. 18, 1997 PCT/US98/27059 Non-provisional of 60/068,006 Dec. 18, 1997 PCT/US98/27059 Non-provisional of 60/068,369 Dec. 19, 1997 PCT/US98/27059 Non-provisional of 60/068,367 Dec. 19, 1997 PCT/US98/27059 Non-provisional of 60/068,368 Dec. 19, 1997 PCT/US98/27059 Non-provisional of 60/068,169 Dec. 19, 1997 PCT/US98/27059 Non-provisional of 60/068,053 Dec. 18, 1997 PCT/US98/27059 Non-provisional of 60/068,064 Dec. 18, 1997 PCT/US98/27059 Non-provisional of 60/068,054 Dec. 18, 1997 PCT/US98/27059 Non-provisional of 60/068,008 Dec. 18, 1997 PCT/US98/27059 Non-provisional of 60/068,365 Dec. 19, 1997 10/100,683 Continuation-in-part of 09/938,671 Aug. 27, 2001 09/938,671 Continuation of 09/739,907 Dec. 20, 2000 09/739,907 Continuation of 09/348,457 Jul. 07, 1999 09/348,457 Continuation-in-part of PCT/US99/00108 Jan. 06, 1999 10/100,683 Continuation-in-part of 09/739,907 Dec. 20, 2000 09/739,907 Continuation of 09/348,457 Jul. 07, 1999 09/348,457 Continuation-in-part of PCT/US99/00108 Jan. 06, 1999 10/100,683 Continuation-in-part of 09/348,457 Jul. 07, 1999 09/348,457 Continuation-in-part of PCT/US99/00108 Jan. 06, 1999 10/100,683 Continuation-in-part of PCT/US99/00108 Jan. 06, 1999 PCT/US99/00108 Non-provisional of 60/070,704 Jan. 07, 1998 PCT/US99/00108 Non-provisional of 60/070,658 Jan. 07, 1998 PCT/US99/00108 Non-provisional of 60/070,692 Jan. 07, 1998 PCT/US99/00108 Non-provisional of 60/070,657 Jan. 07, 1998 10/100,683 Continuation-in-part of 09/949,925 Sep. 12, 2001 09/949,925 Non-provisional of 60/232,150 Sep. 12, 2000 09/949,925 Continuation-in-part of PCT/US99/01621 Jan. 27, 1999 09/949,925 Continuation-in-part of 09/363,044 Jul. 29, 1999 09/363,044 Continuation-in-part of PCT/US99/01621 Jan. 27, 1999 10/100,683 Continuation-in-part of 09/813,153 Mar. 21, 2001 09/813,153 Continuation of 09/363,044 Jul. 29, 1999 09/363,044 Continuation-in-part of PCT/US99/01621 Jan. 27, 1999 10/100,683 Continuation-in-part of 09/363,044 Jul. 29, 1999 09/363,044 Continuation-in-part of PCT/US99/01621 Jan. 27, 1999 10/100,683 Continuation-in-part of PCT/US99/01621 Jan. 27, 1999 PCT/US99/01621 Non-provisional of 60/073,170 Jan. 30, 1998 PCT/US99/01621 Non-provisional of 60/073,167 Jan. 30, 1998 PCT/US99/01621 Non-provisional of 60/073,165 Jan. 30, 1998 PCT/US99/01621 Non-provisional of 60/073,164 Jan. 30, 1998 PCT/US99/01621 Non-provisional of 60/073,162 Jan. 30, 1998 PCT/US99/01621 Non-provisional of 60/073,161 Jan. 30, 1998 PCT/US99/01621 Non-provisional of 60/073,160 Jan. 30, 1998 PCT/US99/01621 Non-provisional of 60/073,159 Jan. 30, 1998 10/100,683 Continuation-in-part of 10/062,548 Feb. 05, 2002 10/062,548 Continuation of 09/369,247 Aug. 05, 1999 09/369,247 Continuation-in-part of PCT/US99/02293 Feb. 04, 1999 10/100,683 Continuation-in-part of 09/369,247 Aug. 05, 1999 09/369,247 Continuation-in-part of PCT/US99/02293 Feb. 04, 1999 10/100,683 Continuation-in-part of PCT/US99/02293 Feb. 04, 1999 PCT/US99/02293 Non-provisional of 60/074,118 Feb. 09, 1998 PCT/US99/02293 Non-provisional of 60/074,157 Feb. 09, 1998 PCT/US99/02293 Non-provisional of 60/074,037 Feb. 09, 1998 PCT/US99/02293 Non-provisional of 60/074,141 Feb. 09, 1998 PCT/US99/02293 Non-provisional of 60/074,341 Feb. 09, 1998 10/100,683 Continuation-in-part of 09/716,129 Nov. 17, 2000 09/716,129 Continuation-in-part of PCT/US99/03939 Feb. 24, 1999 09/716,129 CON 09/382,572 Aug. 25, 1999 09/382,572 Continuation-in-part of PCT/US99/03939 Feb. 24, 1999 10/100,683 Continuation-in-part of PCT/US99/03939 Feb. 24, 1999 PCT/US99/03939 Non-provisional of 60/076,053 Feb. 26, 1998 PCT/US99/03939 Non-provisional of 60/076,051 Feb. 26, 1998 PCT/US99/03939 Non-provisional of 60/076,054 Feb. 26, 1998 PCT/US99/03939 Non-provisional of 60/076,052 Feb. 26, 1998 PCT/US99/03939 Non-provisional of 60/076,057 Feb. 26, 1998 10/100,683 Continuation-in-part of 09/798,889 Mar. 06, 2001 09/798,889 CON 09/393,022 Sep. 09, 1999 09/393,022 Continuation-in-part of PCT/US99/05721 Mar. 11, 1999 10/100,683 Continuation-in-part of PCT/US99/05721 Mar. 11, 1999 PCT/US99/05721 Non-provisional of 60/077,714 Mar. 12, 1998 PCT/US99/05721 Non-provisional of 60/077,686 Mar. 12, 1998 PCT/US99/05721 Non-provisional of 60/077,687 Mar. 12, 1998 PCT/US99/05721 Non-provisional of 60/077,696 Mar. 12, 1998 10/100,683 Continuation-in-part of 09/397,945 Sep. 17, 1999 09/397,945 Continuation-in-part of PCT/US99/05804 Mar. 18, 1999 10/100,683 Continuation-in-part of PCT/US99/05804 Mar. 18, 1999 PCT/US99/05804 Non-provisional of 60/078,566 Mar. 19, 1998 PCT/US99/05804 Non-provisional of 60/078,576 Mar. 19, 1998 PCT/US99/05804 Non-provisional of 60/078,573 Mar. 19, 1998 PCT/US99/05804 Non-provisional of 60/078,574 Mar. 19, 1998 PCT/US99/05804 Non-provisional of 60/078,579 Mar. 19, 1998 PCT/US99/05804 Non-provisional of 60/080,314 Apr. 01, 1998 PCT/US99/05804 Non-provisional of 60/080,312 Apr. 01, 1998 PCT/US99/05804 Non-provisional of 60/078,578 Mar. 19, 1998 PCT/US99/05804 Non-provisional of 60/078,581 Mar. 19, 1998 PCT/US99/05804 Non-provisional of 60/078,577 Mar. 19, 1998 PCT/US99/05804 Non-provisional of 60/078,563 Mar. 19, 1998 PCT/US99/05804 Non-provisional of 60/080,313 Apr. 01, 1998 10/100,683 Continuation-in-part of 09/948,783 Sep. 10, 2001 09/948,783 Non-provisional of 60/231,846 Sep. 11, 2000 09/948,783 Continuation-in-part of 09/892,877 Jun. 28, 2001 09/892,877 Continuation of 09/437,658 Nov. 10, 1999 09/437,658 Continuation-in-part of PCT/US99/09847 May 06, 1999 10/100,683 Continuation-in-part of 09/892,877 Jun. 28, 2001 09/892,877 Continuation of 09/437,658 Nov. 10, 1999 09/437,658 Continuation-in-part of PCT/US99/09847 May 06, 1999 10/100,683 Continuation-in-part of PCT/US99/09847 May 06, 1999 PCT/US99/09847 Non-provisional of 60/085,093 May 12, 1998 PCT/US99/09847 Non-provisional of 60/085,094 May 12, 1998 PCT/US99/09847 Non-provisional of 60/085,105 May 12, 1998 PCT/US99/09847 Non-provisional of 60/085,180 May 12, 1998 PCT/US99/09847 Non-provisional of 60/085,927 May 18, 1998 PCT/US99/09847 Non-provisional of 60/085,906 May 18, 1998 PCT/US99/09847 Non-provisional of 60/085,920 May 18, 1998 PCT/US99/09847 Non-provisional of 60/085,924 May 18, 1998 PCT/US99/09847 Non-provisional of 60/085,922 May 18, 1998 PCT/US99/09847 Non-provisional of 60/085,923 May 18, 1998 PCT/US99/09847 Non-provisional of 60/085,921 May 18, 1998 PCT/US99/09847 Non-provisional of 60/085,925 May 18, 1998 PCT/US99/09847 Non-provisional of 60/085,928 May 18, 1998 10/100,683 Continuation-in-part of 10/050,873 Jan. 18, 2002 10/050,873 Non-provisional of 60/263,681 Jan. 24, 2001 10/050,873 Non-provisional of 60/263,230 Jan. 23, 2001 10/050,873 Continuation-in-part of 09/461,325 Dec. 14, 1999 09/461,325 Continuation-in-part of PCT/US99/13418 Jun. 15, 1999 10/100,683 Continuation-in-part of 10/012,542 Dec. 12, 2001 10/012,542 Divisional of 09/461,325 Dec. 14, 1999 09/461,325 Continuation-in-part of PCT/US99/13418 Jun. 15, 1999 10/100,683 Continuation-in-part of 09/461,325 Dec. 14, 1999 09/461,325 Continuation-in-part of PCT/US99/13418 Jun. 15, 1999 10/100,683 Continuation-in-part of PCT/US99/13418 Jun. 15, 1999 PCT/US99/13418 Non-provisional of 60/089,507 Jun. 16, 1998 PCT/US99/13418 Non-provisional of 60/089,508 Jun. 16, 1998 PCT/US99/13418 Non-provisional of 60/089,509 Jun. 16, 1998 PCT/US99/13418 Non-provisional of 60/089,510 Jun. 16, 1998 PCT/US99/13418 Non-provisional of 60/090,112 Jun. 22, 1998 PCT/US99/13418 Non-provisional of 60/090,113 Jun. 22, 1998 10/100,683 Continuation-in-part of 09/984,271 Oct. 29, 2001 09/984,271 Divisional of 09/482,273 Jan. 13, 2000 09/482,273 Continuation-in-part of PCT/US99/15849 Jul. 14, 1999 10/100,683 Continuation-in-part of 09/984,276 Oct. 29, 2001 09/984,276 Divisional of 09/482,273 Jan. 13, 2000 09/482,273 Continuation-in-part of PCT/US99/15849 Jul. 14, 1999 10/100,683 Continuation-in-part of 09/482,273 Jan. 13, 2000 09/482,273 Continuation-in-part of PCT/US99/15849 Jul. 14, 1999 10/100,683 Continuation-in-part of PCT/US99/15849 Jul. 14, 1999 PCT/US99/15849 Non-provisional of 60/092,921 Jul. 15, 1998 PCT/US99/15849 Non-provisional of 60/092,922 Jul. 15, 1998 PCT/US99/15849 Non-provisional of 60/092,956 Jul. 15, 1998 10/100,683 Continuation-in-part of PCT/US01/29871 Sep. 24, 2001 PCT/US01/29871 Non-provisional of 60/234,925 Sep. 25, 2000 PCT/US01/29871 Continuation-in-part of PCT/US01/00911 Jan. 12, 2001 10/100,683 Continuation-in-part of PCT/US01/00911 Jan. 12, 2001 PCT/US01/00911 Continuation-in-part of 09/482,273 Jan. 13, 2000 10/100,683 Non-provisional of 60/350,898 Jan. 25, 2002 10/100,683 Continuation-in-part of 09/489,847 Jan. 24, 2000 09/489,847 Continuation-in-part of PCT/US99/17130 Jul. 29, 1999 10/100,683 Continuation-in-part of PCT/US99/17130 Jul. 29, 1999 PCT/US99/17130 Non-provisional of 60/094,657 Jul. 30, 1998 PCT/US99/17130 Non-provisional of 60/095,486 Aug. 05, 1998 PCT/US99/17130 Non-provisional of 60/096,319 Aug. 12, 1998 PCT/US99/17130 Non-provisional of 60/095,454 Aug. 06, 1998 PCT/US99/17130 Non-provisional of 60/095,455 Aug. 06, 1998 10/100,683 Continuation-in-part of 10/054,988 Jan. 25, 2002 10/054,988 Continuation of 09/904,615 Jul. 16, 2001 09/904,615 Continuation of 09/739,254 Dec. 19, 2000 09/739,254 Continuation of 09/511,554 Feb. 23, 2000 09/511,554 Continuation-in-part of PCT/US99/19330 Aug. 24, 1999 10/100,683 Continuation-in-part of 09/904,615 Jul. 16, 2001 09/904,615 Continuation of 09/739,254 Dec. 19, 2000 09/739,254 Continuation of 09/511,554 Feb. 23, 2000 09/511,554 Continuation-in-part of PCT/US99/19330 Aug. 24, 1999 10/100,683 Continuation-in-part of PCT/US99/19330 Aug. 24, 1999 PCT/US99/19330 Non-provisional of 60/097,917 Aug. 25, 1998 PCT/US99/19330 Non-provisional of 60/098,634 Aug. 31, 1998 10/100,683 Continuation-in-part of 09/820,893 Mar. 30, 2001 09/820,893 Continuation of 09/531,119 Mar. 20, 2000 09/531,119 Continuation-in-part of PCT/US99/22012 Sep. 22, 1999 10/100,683 Continuation-in-part of PCT/US99/22012 Sep. 22, 1999 PCT/US99/22012 Non-provisional of 60/101,546 Sep. 23, 1998 PCT/US99/22012 Non-provisional of 60/102,895 Oct. 02, 1998 10/100,683 Continuation-in-part of 09/948,820 Sep. 10, 2001 09/948,820 Continuation of 09/565,391 May 05, 2000 09/565,391 Continuation-in-part of PCT/US99/26409 Nov. 09, 1999 10/100,683 Continuation-in-part of 09/565,391 May 05, 2000 09/565,391 Continuation-in-part of PCT/US99/26409 Nov. 09, 1999 10/100,683 Continuation-in-part of PCT/US99/26409 Nov. 09, 1999 PCT/US99/26409 Non-provisional of 60/108,207 Nov. 12, 1998 10/100,683 Continuation-in-part of 09/895,298 Jul. 02, 2001 09/895,298 Continuation of 09/591,316 Jun. 09, 2000 09/591,316 Continuation-in-part of PCT/US99/29950 Dec. 16, 1999 10/100,683 Continuation-in-part of PCT/US99/29950 Dec. 16, 1999 PCT/US99/29950 Non-provisional of 60/113,006 Dec. 18, 1998 PCT/US99/29950 Non-provisional of 60/112,809 Dec. 17, 1998 10/100,683 Continuation-in-part of 09/985,153 Nov. 01, 2001 09/985,153 Continuation of 09/618,150 Jul. 17, 2000 09/618,150 Continuation-in-part of PCT/US00/00903 Jan. 18, 2000 10/100,683 Continuation-in-part of PCT/US00/00903 Jan. 18, 2000 PCT/US00/00903 Non-provisional of 60/116,330 Jan. 19, 1999 10/100,683 Continuation-in-part of 09/997,131 Nov. 30, 2001 09/997,131 Continuation of 09/628,508 Jul. 28, 2000 09/628,508 Continuation-in-part of PCT/US00/03062 Feb. 08, 2000 10/100,683 Continuation-in-part of PCT/US00/03062 Feb. 08, 2000 PCT/US00/03062 Non-provisional of 60/119,468 Feb. 10, 1999 10/100,683 Continuation-in-part of 10/050,882 Jan. 18, 2002 10/050,882 Continuation of 09/661,453 Sep. 13, 2000 09/661,453 Continuation-in-part of PCT/US00/06783 Mar. 16, 2000 10/100,683 Continuation-in-part of 09/661,453 Sep. 13, 2000 09/661,453 Continuation-in-part of PCT/US00/06783 Mar. 16, 2000 10/100,683 Continuation-in-part of PCT/US00/06783 Mar. 16, 2000 PCT/US00/06783 Non-provisional of 60/125,055 Mar. 18, 1999 10/100,683 Continuation-in-part of 10/050,704 Jan. 18, 2002 10/050,704 Continuation of 09/684,524 Oct. 10, 2000 09/684,524 Continuation-in-part of PCT/US00/08979 Apr. 06, 2000 10/100,683 Continuation-in-part of 09/684,524 Oct. 10, 2000 09/684,524 Continuation-in-part of PCT/US00/08979 Apr. 06, 2000 10/100,683 Continuation-in-part of PCT/US00/08979 Apr. 06, 2000 PCT/US00/08979 Non-provisional of 60/128,693 Apr. 09, 1999 PCT/US00/08979 Non-provisional of 60/130,991 Apr. 26, 1999 10/100,683 Continuation-in-part of 10/042,141 Jan. 11, 2002 10/042,141 Continuation of 09/726,643 Dec. 01, 2000 09/726,643 Continuation-in-part of PCT/US00/15187 Jun. 02, 2000 10/100,683 Continuation-in-part of 09/726,643 Dec. 01, 2000 09/726,643 Continuation-in-part of PCT/US00/15187 Jun. 02, 2000 10/100,683 Continuation-in-part of PCT/US00/15187 Jun. 02, 2000 PCT/US00/15187 Non-provisional of 60/137,725 Jun. 07, 1999 10/100,683 Continuation-in-part of 09/756,168 Jan. 09, 2001 09/756,168 Continuation-in-part of PCT/US00/19735 Jul. 23, 1999 10/100,683 Continuation-in-part of PCT/US00/19735 Jul. 20, 2000 PCT/US00/19735 Non-provisional of 60/145,220 Jul. 23, 1999 10/100,683 Continuation-in-part of PZ042P1C1 Feb. 01, 2002 PZ042P1C1 Continuation of 09/781,417 Feb. 13, 2001 09/781,417 Continuation-in-part of PCT/US00/22325 Aug. 16, 2000 10/100,683 Continuation-in-part of 09/781,417 Feb. 13, 2001 09/781,417 Continuation-in-part of PCT/US00/22325 Aug. 16, 2000 10/100,683 Continuation-in-part of PCT/US00/22325 Aug. 16, 2000 PCT/US00/22325 Non-provisional of 60/149,182 Aug. 17, 1999 10/100,683 Continuation-in-part of 09/789,561 Feb. 22, 2001 09/789,561 Continuation-in-part of PCT/US00/24008 Aug. 31, 2000 10/100,683 Continuation-in-part of PCT/US00/24008 Aug. 31, 2000 PCT/US00/24008 Non-provisional of 60/152,315 Sep. 03, 1999 PCT/US00/24008 Non-provisional of 60/152,317 Sep. 03, 1999 10/100,683 Continuation-in-part of 09/800,729 Mar. 08, 2001 09/800,729 Continuation-in-part of PCT/US00/26013 Sep. 22, 2000 10/100,683 Continuation-in-part of PCT/US00/26013 Sep. 22, 2000 PCT/US00/26013 Non-provisional of 60/155,709 Sep. 24, 1999 10/100,683 Continuation-in-part of 09/832,129 Apr. 11, 2001 09/832,129 Continuation-in-part of PCT/US00/28664 Oct. 17, 2000 10/100,683 Continuation-in-part of PCT/US00/28664 Oct. 17, 2000 PCT/US00/28664 Non-provisional of 60/163,085 Nov. 02, 1999 PCT/US00/28664 Non-provisional of 60/172,411 Dec. 17, 1999 10/100,683 Continuation-in-part of PCT/US00/29363 Oct. 25, 2000 PCT/US00/29363 Non-provisional of 60/215,139 Jun. 30, 2000 PCT/US00/29363 Non-provisional of 60/162,239 Oct. 29, 1999 10/100,683 Continuation-in-part of PCT/US00/29360 Oct. 25, 2000 PCT/US00/29360 Non-provisional of 60/215,138 Jun. 30, 2000 PCT/US00/29360 Non-provisional of 60/162,211 Oct. 29, 1999 10/100,683 Continuation-in-part of PCT/US00/29362 Oct. 25, 2000 PCT/US00/29362 Non-provisional of 60/215,131 Jun. 30, 2000 PCT/US00/29362 Non-provisional of 60/162,240 Oct. 29, 1999 10/100,683 Continuation-in-part of PCT/US00/29365 Oct. 25, 2000 PCT/US00/29365 Non-provisional of 60/219,666 Jul. 21, 2000 PCT/US00/29365 Non-provisional of 60/162,237 Oct. 29, 1999 10/100,683 Continuation-in-part of PCT/US00/29364 Oct. 25, 2000 PCT/US00/29364 Non-provisional of 60/215,134 Jun. 30, 2000 PCT/US00/29364 Non-provisional of 60/162,238 Oct. 29, 1999 10/100,683 Continuation-in-part of PCT/US00/30040 Nov. 01, 2000 PCT/US00/30040 Non-provisional of 60/215,130 Jun. 30, 2000 PCT/US00/30040 Non-provisional of 60/163,580 Nov. 05, 1999 10/100,683 Continuation-in-part of PCT/US00/30037 Nov. 01, 2000 PCT/US00/30037 Non-provisional of 60/215,137 Jun. 30, 2000 PCT/US00/30037 Non-provisional of 60/163,577 Nov. 05, 1999 10/100,683 Continuation-in-part of PCT/US00/30045 Nov. 01, 2000 PCT/US00/30045 Non-provisional of 60/215,133 Jun. 30, 2000 PCT/US00/30045 Non-provisional of 60/163,581 Nov. 05, 1999 10/100,683 Continuation-in-part of PCT/US00/30036 Nov. 01, 2000 PCT/US00/30036 Non-provisional of 60/221,366 Jul. 27, 2000 PCT/US00/30036 Non-provisional of 60/163,576 Nov. 05, 1999 10/100,683 Continuation-in-part of PCT/US00/30039 Nov. 01, 2000 PCT/US00/30039 Non-provisional of 60/221,367 Jul. 27, 2000 PCT/US00/30039 Non-provisional of 60/195,296 Apr. 07, 2000 PCT/US00/30039 Non-provisional of 60/164,344 Nov. 09, 1999 10/100,683 Continuation-in-part of PCT/US00/30654 Nov. 08, 2000 PCT/US00/30654 Non-provisional of 60/221,142 Jul. 27, 2000 PCT/US00/30654 Non-provisional of 60/164,835 Nov. 12, 1999 10/100,683 Continuation-in-part of PCT/US00/30628 Nov. 08, 2000 PCT/US00/30628 Non-provisional of 60/215,140 Jun. 30, 2000 PCT/US00/30628 Non-provisional of 60/164,744 Nov. 12, 1999 10/100,683 Continuation-in-part of PCT/US00/30653 Nov. 08, 2000 PCT/US00/30653 Non-provisional of 60/221,193 Jul. 27, 2000 PCT/US00/30653 Non-provisional of 60/164,735 Nov. 12, 1999 10/100,683 Continuation-in-part of PCT/US00/30629 Nov. 08, 2000 PCT/US00/30629 Non-provisional of 60/222,904 Aug. 03, 2000 PCT/US00/30629 Non-provisional of 60/164,825 Nov. 12, 1999 10/100,683 Continuation-in-part of PCT/US00/30679 Nov. 08, 2000 PCT/US00/30679 Non-provisional of 60/224,007 Aug. 04, 2000 PCT/US00/30679 Non-provisional of 60/164,834 Nov. 12, 1999 10/100,683 Continuation-in-part of PCT/US00/30674 Nov. 08, 2000 PCT/US00/30674 Non-provisional of 60/215,128 Jun. 30, 2000 PCT/US00/30674 Non-provisional of 60/164,750 Nov. 12, 1999 10/100,683 Continuation-in-part of PCT/US00/31162 Nov. 15, 2000 60/215,136 Non-provisional of 60/215,136 Jun. 30, 2000 60/215,136 Non-provisional of 60/166,415 Nov. 19, 1999 10/100,683 Continuation-in-part of PCT/US00/31282 Nov. 15, 2000 PCT/US00/31282 Non-provisional of 60/219,665 Jul. 21, 2000 PCT/US00/31282 Non-provisional of 60/166,414 Nov. 19, 1999 10/100,683 Continuation-in-part of PCT/US00/30657 Nov. 08, 2000 PCT/US00/30657 Non-provisional of 60/215,132 Jun. 30, 2000 PCT/US00/30657 Non-provisional of 60/164,731 Nov. 12, 1999 10/100,683 Continuation-in-part of PCT/US01/01396 Jan. 17, 2001 60/256,968 Non-provisional of 60/256,968 Dec. 21, 2000 60/256,968 Non-provisional of 60/226,280 Aug. 18, 2000 10/100,683 Continuation-in-part of PCT/US01/01387 Jan. 17, 2001 60/259,803 Non-provisional of 60/259,803 Jan. 05, 2001 60/259,803 Non-provisional of 60/226,380 Aug. 18, 2000 10/100,683 Continuation-in-part of PCT/US01/01567 Jan. 17, 2001 PCT/US01/01567 Non-provisional of 60/228,084 Aug. 28, 2000 10/100,683 Continuation-in-part of PCT/US01/01431 Jan. 17, 2001 PCT/US01/01431 Non-provisional of 60/231,968 Sep. 12, 2000 PCT/US01/01431 Continuation-in-part of 09/915,582 Jul. 27, 2001 10/100,683 Continuation-in-part of PCT/US01/01432 Jan. 17, 2001 PCT/US01/01432 Non-provisional of 60/236,326 Sep. 29, 2000 10/100,683 Continuation-in-part of PCT/US01/00544 Jan. 09, 2001 PCT/US01/00544 Non-provisional of 60/234,211 Sep. 20, 2000 10/100,683 Continuation-in-part of PCT/US01/01435 Jan. 17, 2001 PCT/US01/01435 Non-provisional of 60/226,282 Aug. 18, 2000 10/100,683 Continuation-in-part of PCT/US01/01386 Jan. 17, 2001 PCT/US01/01386 Non-provisional of 60/232,104 Sep. 12, 2000 10/100,683 Continuation-in-part of PCT/US01/01565 Jan. 17, 2001 PCT/US01/01565 Non-provisional of 60/234,210 Sep. 20, 2000 10/100,683 Continuation-in-part of PCT/US01/01394 Jan. 17, 2001 PCT/US01/01394 Non-provisional of 60/259,805 Jan. 05, 2001 PCT/US01/01394 Non-provisional of 60/226,278 Aug. 18, 2000 10/100,683 Continuation-in-part of PCT/US01/01434 Jan. 17, 2001 PCT/US01/01434 Non-provisional of 60/259,678 Jan. 05, 2001 PCT/US01/01434 Non-provisional of 60/226,279 Aug. 18, 2000 10/100,683 Continuation-in-part of PCT/US01/01397 Jan. 17, 2001 PCT/US01/01397 Non-provisional of 60/226,281 Aug. 18, 2000 10/100,683 Continuation-in-part of PCT/US01/01385 Jan. 17, 2001 PCT/US01/01385 Non-provisional of 60/231,969 Sep. 12, 2000 10/100,683 Continuation-in-part of PCT/US01/01384 Jan. 17, 2001 PCT/US01/01384 Non-provisional of 60/259,516 Jan. 04, 2001 PCT/US01/01384 Non-provisional of 60/228,086 Aug. 28, 2000 10/100,683 Continuation-in-part of PCT/US01/01383 Jan. 17, 2001 PCT/US01/01383 Non-provisional of 60/259,804 Jan. 05, 2001 PCT/US01/01383 Non-provisional of 60/228,083 Aug. 28, 2000 10/100,683 Continuation-in-part of PCT/US02/05064 Feb. 21, 2002 PCT/US02/05064 Non-provisional of 60/304,444 Jul. 12, 2001 PCT/US02/05064 Non-provisional of 60/270,658 Feb. 23, 2001 10/100,683 Continuation-in-part of PCT/US02/05301 Feb. 21, 2002 PCT/US02/05301 Non-provisional of 60/304,417 Jul. 12, 2001 PCT/US02/05301 Non-provisional of 60/270,625 Feb. 23, 2001 10/100,683 Non-provisional of 60/304,121 Jul. 11, 2001 10/100,683 Non-provisional of 60/295,869 Jun. 06, 2001 10/100,683 Non-provisional of 60/325,209 Sep. 28, 2001 10/100,683 Non-provisional of 60/311,085 Aug. 10, 2001 10/100,683 Non-provisional of 60/330,629 Oct. 26, 2001 10/100,683 Non-provisional of 60/331,046 Nov. 07, 2001 10/100,683 Non-provisional of 60/358,554 Feb. 22, 2002 10/100,683 Non-provisional of 60/358,714 Feb. 25, 2002 ; wherein each of the above applications are all herein incorporated by reference in their entirety.

FIELD OF THE INVENTION

The present invention relates to human secreted proteins/polypeptides, and isolated nucleic acid molecules encoding said proteins/polypeptides, useful for detecting, preventing, diagnosing, prognosticating, treating, and/or ameliorating cancer and other hyperproliferative disorders. Antibodies that bind these polypeptides are also encompassed by the present invention. Also encompassed by the invention are vectors, host cells, and recombinant and synthetic methods for producing said polynucleotides, polypeptides, and/or antibodies. The invention further encompasses screening methods for identifying agonists and antagonists of polynucleotides and polypeptides of the invention. The present invention further encompasses methods and compositions for inhibiting or enhancing the production and function of the polypeptides of the present invention.

BACKGROUND OF THE INVENTION

Cancer and other hyperproliferative disorders are a diverse group of disorders and diseases sharing one characteristic in common; all result from uncontrolled cell proliferation. The human body is composed of many different cell types, e.g. liver cells, muscle cells, brain cells, etc. Normally, these cells grow and divide to produce more cells only as the body needs them (e.g. to regenerate blood cells or replace epithelial cells lining the stomach). Sometimes, however, cells begin to divide unchecked even though new cells are not needed. These extra cells accumulate and form a mass of tissue, called a tumor. Although each of the over 200 cell types in the body can potentially become cancerous, some cell types become cancerous at relatively high rates while many other cell types rarely become cancerous.

Tumors are either benign or malignant. Benign tumors are not cancerous; they can usually be removed, they do not spread to other parts of the body and, they rarely threaten life. Malignant tumors, however, are cancerous. Cells in malignant tumors can invade and damage nearby or distant tissues and organs. The spread of cancerous cells is called metastasis. Malignant (or metastatic) cells can invade adjacent organs by proliferating directly from the primary tumor. Additionally, malignant cells can also metastasize to distant organs by breaking away from the primary tumor, entering the bloodstream or lymphatic system, and settling down in a new organ or tissue to produce a secondary tumor. The origin of secondary tumors is established by comparing cells comprising these tumors to cells in the original (primary) tumor.

In contrast to solid organ cancers (such as cancer in the liver, lung, and brain) cancer can also develop in blood-forming cells. These cancers are referred to as leukemias or lymphomas. Leukemia refers to cancer of blood forming cells such as red blood cells, platelets, and plasma cells. Lymphomas are a subset of leukemias, primarily involving white blood cells, in which the cancerous cells originated in, or are associated with, the lymph system and lymph organs (e.g. T-lymphocytes in the lymph nodes, spleen, or thymus).

In 1999 over 1.1 million people were newly diagnosed with 23 different types of cancer. The vast majority of these cases (˜75%) involved cancers of the prostate, breast, lung, colon, or urinary tract, or non-Hodgkin's lymphoma. Among the most fatal cancers are pancreatic, liver, esophageal, lung, stomach, and brain cancers, having up to 96% mortality rates depending on the specific cancer. In all, some 23 different types of cancer are expected to kill over 86,000 people each year.

Most cancers are treated with one or a combination therapies consisting of surgery, radiation therapy, chemotherapy, hormone therapy, and/or biological therapy. These five therapeutic modes are either local or systemic treatment strategies. Local treatments affect cancer cells in the tumor and immediately adjacent areas (for example, surgical tumor removal is a local treatment as are most radiation treatments). In contrast, systemic treatments travel through the bloodstream, and reach cancer and other cells all over the body. Chemotherapy, hormone therapy, and biological therapy are examples of systemic treatments.

Whether systemic or local, it is often difficult or impossible to protect healthy cells from the harmful effects of cancer treatment; healthy cells and tissues are inevitably damaged in the process of treating the cancerous cells. Damage and disruption of the normal functioning of healthy cells and tissues often produces the undesirable side effects experienced by patients undergoing cancer treatment.

Recombinant polypeptides and polynucleotides derived from naturally occurring molecules, as well as antibodies specifically targeted to these molecules, used alone or in conjunction with other existing therapies, hold great promise as improved therapeutic agents for the treatment of neoplastic disorders. Currently, most biological therapy can be classified as immunotherapy because these treatments often use naturally occurring molecules to assist the body's immune system in fighting the disease or in protecting the body from side effects of other cancer treatment(s). Among the most commonly used compounds in biological therapies are proteins called cytokines (e.g. interferons, interleukins, and colony stimulating factors) and monoclonal antibodies (targeted to particular cancer cells). Side effects caused by these commonly used biological therapies range from flu-like symptoms (chills, fever, muscle aches, weakness, loss of appetite, nausea, vomiting, and diarrhea) to rashes, swelling, easy bruising, or bleeding.

The discovery of human secreted proteins associated with initiation, progression, characterization, and/or distinction of neoplastic diseases (including antibodies that immunospecifically bind these polypeptides), satisfies a need in the art by providing new compositions useful in the detection, prevention, diagnosis, treatment, prevention, prognosis, and treatment of hyperproliferative disorders.

SUMMARY OF THE INVENTION

The present invention encompasses human secreted proteins/polypeptides, and isolated nucleic acid molecules encoding said proteins/polypeptides, useful for detecting, preventing, diagnosing, prognosticating, treating, and/or ameliorating cancer and other hyperproliferative disorders. Antibodies that bind these polypeptides are also encompassed by the present invention; as are vectors, host cells, and recombinant and synthetic methods for producing said polynucleotides, polypeptides, and/or antibodies. The invention further encompasses screening methods for identifying agonists and antagonists of polynucleotides and polypeptides of the invention. The present invention also encompasses methods and compositions for inhibiting or enhancing the production and function of the polypeptides of the present invention.

DETAILED DESCRIPTION

Polynucleotides and Polypeptides of the Invention

Description of Table 1A

Table 1A summarizes information concerning certain polynucleotides and polypeptides of the invention. The first column provides the gene number in the application for each clone identifier. The second column provides a unique clone identifier, “Clone ID:”, for a cDNA clone related to each contig sequence disclosed in Table 1A. Third column, the cDNA Clones identified in the second column were deposited as indicated in the third column (i.e. by ATCC™ Deposit No:Z and deposit date). Some of the deposits contain multiple different clones corresponding to the same gene. In the fourth column, “Vector” refers to the type of vector contained in the corresponding cDNA Clone identified in the second column. In the fifth column, the nucleotide sequence identified as “NT SEQ ID NO:X” was assembled from partially homologous (“overlapping”) sequences obtained from the corresponding cDNA clone identified in the second column and, in some cases, from additional related cDNA clones. The overlapping sequences were assembled into a single contiguous sequence of high redundancy (usually three to five overlapping sequences at each nucleotide position), resulting in a final sequence identified as SEQ ID NO:X. In the sixth column, “Total NT Seq.” refers to the total number of nucleotides in the contig sequence identified as SEQ ID NO:X.” The deposited clone may contain all or most of these sequences, reflected by the nucleotide position indicated as “5′ NT of Clone Seq.” (seventh column) and the “3′ NT of Clone Seq.” (eighth column) of SEQ ID NO:X. In the ninth column, the nucleotide position of SEQ ID NO:X of the putative start codon (methionine) is identified as “5′ NT of Start Codon.” Similarly, in column ten, the nucleotide position of SEQ ID NO:X of the predicted signal sequence is identified as “5′ NT of First AA of Signal Pep.” In the eleventh column, the translated amino acid sequence, beginning with the methionine, is identified as “AA SEQ ID NO:Y,” although other reading frames can also be routinely translated using known molecular biology techniques. The polypeptides produced by these alternative open reading frames are specifically contemplated by the present invention.

In the twelfth and thirteenth columns of Table 1A, the first and last amino acid position of SEQ ID NO:Y of the predicted signal peptide is identified as “First AA of Sig Pep” and “Last AA of Sig Pep.” In the fourteenth column, the predicted first amino acid position of SEQ ID NO:Y of the secreted portion is identified as “Predicted First AA of Secreted Portion”. The amino acid position of SEQ ID NO:Y of the last amino acid encoded by the open reading frame is identified in the fifteenth column as “Last AA of ORF”.

SEQ ID NO:X (where X may be any of the polynucleotide sequences disclosed in the sequence listing) and the translated SEQ ID NO:Y (where Y may be any of the polypeptide sequences disclosed in the sequence listing) are sufficiently accurate and otherwise suitable for a variety of uses well known in the art and described further below. For instance, SEQ ID NO:X is useful for designing nucleic acid hybridization probes that will detect nucleic acid sequences contained in SEQ ID NO:X or the cDNA contained in the deposited clone. These probes will also hybridize to nucleic acid molecules in biological samples, thereby enabling a variety of forensic and diagnostic methods of the invention. Similarly, polypeptides identified from SEQ ID NO:Y may be used, for example, to generate antibodies which bind specifically to proteins containing the polypeptides and the secreted proteins encoded by the cDNA clones identified in Table 1A and/or elsewhere herein

Nevertheless, DNA sequences generated by sequencing reactions can contain sequencing errors. The errors exist as misidentified nucleotides, or as insertions or deletions of nucleotides in the generated DNA sequence. The erroneously inserted or deleted nucleotides cause frame shifts in the reading frames of the predicted amino acid sequence. In these cases, the predicted amino acid sequence diverges from the actual amino acid sequence, even though the generated DNA sequence may be greater than 99.9% identical to the actual DNA sequence (for example, one base insertion or deletion in an open reading frame of over 1000 bases).

Accordingly, for those applications requiring precision in the nucleotide sequence or the amino acid sequence, the present invention provides not only the generated nucleotide sequence identified as SEQ ID NO:X, and the predicted translated amino acid sequence identified as SEQ ID NO:Y, but also a sample of plasmid DNA containing a human cDNA of the invention deposited with the ATCC™, as set forth in Table 1A. The nucleotide sequence of each deposited plasmid can readily be determined by sequencing the deposited plasmid in accordance with known methods

The predicted amino acid sequence can then be verified from such deposits. Moreover, the amino acid sequence of the protein encoded by a particular plasmid can also be directly determined by peptide sequencing or by expressing the protein in a suitable host cell containing the deposited human cDNA, collecting the protein, and determining its sequence.

Also provided in Table 1A is the name of the vector which contains the cDNA plasmid. Each vector is routinely used in the art. The following additional information is provided for convenience.

Vectors Lambda Zap (U.S. Pat. Nos. 5,128,256 and 5,286,636), Uni-Zap XR (U.S. Pat. Nos. 5,128,256 and 5,286,636), Zap Express (U.S. Pat. Nos. 5,128,256 and 5,286,636), pBLUESCRIPT™ (pBS) (Short, J. M. et al., Nucleic Acids Res. 16:7583-7600 (1988); Alting-Mees, M. A. and Short, J. M., Nucleic Acids Res. 17.9494 (1989)) and pBK (Alting-Mees, M. A. et al., Strategies 5:58-61 (1992)) are commercially available from STRATAGENE™ Cloning Systems, Inc., 11011 N. Torrey Pines Road, La Jolla, Calif., 92037. pBS contains an ampicillin resistance gene and pBK contains a neomycin resistance gene. Phagemid pBS may be excised from the Lambda Zap and Uni-Zap XR vectors, and phagemid pBK may be excised from the Zap Express vector. Both phagemids may be transformed into E. coli strain XL-1 Blue, also available from STRATAGENE™

Vectors pSport1, pCMVSport 1.0, pCMVSport 2.0 and pCMVSport 3.0, were obtained from LIFE TECHNOLOGIES™, Inc., P.O. Box 6009, Gaithersburg, Md. 20897. All Sport vectors contain an ampicillin resistance gene and may be transformed into E. coli strain DH10B, also available from LIFE TECHNOLOGIES™. See, for instance, Gruber, C. E., et al., Focus 15.59 (1993). Vector lafmid BA (Bento Soares, Columbia University, New York, N.Y.) contains an ampicillin resistance gene and can be transformed into E. coli strain XL-1 Blue. Vector pCR®2.1, which is available from Invitrogen, 1600 Faraday Avenue, Carlsbad, Calif. 92008, contains an ampicillin resistance gene and may be transformed into E. coli strain DH10B, available from LIFE TECHNOLOGIES™. See, for instance, Clark, J. M., Nuc. Acids Res. 16:9677-9686 (1988) and Mead, D. et al, Bio/Technology 9. (1991).

The present invention also relates to the genes corresponding to SEQ ID NO:X, SEQ ID NO:Y, and/or a deposited cDNA (cDNA Clone ID). The corresponding gene can be isolated in accordance with known methods using the sequence information disclosed herein. Such methods include, but are not limited to, preparing probes or primers from the disclosed sequence and identifying or amplifying the corresponding gene from appropriate sources of genomic material.

Also provided in the present invention are allelic variants, orthologs, and/or species homologs. Procedures known in the art can be used to obtain full-length genes, allelic variants, splice variants, full-length coding portions, orthologs, and/or species homologs of genes corresponding to SEQ ID NO:X and SEQ ID NO:Y using information from the sequences disclosed herein or the clones deposited with the ATCC™. For example, allelic variants and/or species homologs may be isolated and identified by making suitable probes or primers from the sequences provided herein and screening a suitable nucleic acid source for allelic variants and/or the desired homologue.

The present invention provides a polynucleotide comprising, or alternatively consisting of, the nucleic acid sequence of SEQ ID NO:X and/or a cDNA contained in ATCC™ Deposit No.Z. The present invention also provides a polypeptide comprising, or alternatively, consisting of, the polypeptide sequence of SEQ ID NO:Y, a polypeptide encoded by SEQ ID NO:X, and/or a polypeptide encoded by a cDNA contained in ATCC™ deposit No.Z. Polynucleotides encoding a polypeptide comprising, or alternatively consisting of the polypeptide sequence of SEQ ID NO:Y, a polypeptide encoded by SEQ ID NO:X and/or a polypeptide encoded by the cDNA contained in ATCC™ Deposit No.Z, are also encompassed by the invention. The present invention further encompasses a polynucleotide comprising, or alternatively consisting of the complement of the nucleic acid sequence of SEQ ID NO:X, and/or the complement of the coding strand of the cDNA contained in ATCC™ Deposit No.Z.

Description of Table 1B (Comprised of Tables 1B.1 and 1B.2)

Table 1B.1 and Table 1B.2 summarize some of the polynucleotides encompassed by the invention (including cDNA clones related to the sequences (Clone ID:), contig sequences (contig identifier (Contig ID:) and contig nucleotide sequence identifiers (SEQ ID NO:X)) and further summarizes certain characteristics of these polynucleotides and the polypeptides encoded thereby. The first column of Tables 1B.1 and 1B.2 provide the gene numbers in the application for each clone identifier. The second column of Tables 1B.1 and 1B.2 provide unique clone identifiers, “Clone ID:”, for cDNA clones related to each contig sequence disclosed in Table 1A and/or Table 1B. The third column of Tables 1B.1 and 1B.2 provide unique contig identifiers, “Contig ID:” for each of the contig sequences disclosed in these tables. The fourth column of Tables 1B.1 and 1B.2 provide the sequence identifiers, “SEQ ID NO:X”, for each of the contig sequences disclosed in Table 1A and/or 1B.

Table 1B.1

The fifth column of Table 1B.1, “ORF (From-To)”, provides the location (i.e., nucleotide position numbers) within the polynucleotide sequence of SEQ ID NO:X that delineates the preferred open reading frame (ORF) that encodes the amino acid sequence shown in the sequence listing and referenced in Table 1B.1 as SEQ ID NO:Y (column 6). Column 7 of Table B.1 lists residues comprising predicted epitopes contained in the polypeptides encoded by each of the preferred ORFs (SEQ ID NO:Y). Identification of potential immunogenic regions was performed according to the method of Jameson and Wolf (CABIOS, 4; 181-186 (1988)); specifically, the Genetics Computer Group (GCG) implementation of this algorithm, embodied in the program PEPTIDESTRUCTURE (Wisconsin Package v10.0, Genetics Computer Group (GCG), Madison, Wisc.). This method returns a measure of the probability that a given residue is found on the surface of the protein. Regions where the antigenic index score is greater than 0.9 over at least 6 amino acids are indicated in Table 1B.1 as “Predicted Epitopes”. In particular embodiments, polypeptides of the invention comprise, or alternatively consist of, one, two, three, four, five or more of the predicted epitopes described in Table B.1. It will be appreciated that depending on the analytical criteria used to predict antigenic determinants, the exact address of the determinant may vary slightly. Column 8 of Table 1B.1 (“Tissue Distribution”) is described below in Table 1B.2 Column 5. Column 9 of Table 1B.1 (“Cytologic Band”) provides the chromosomal location of polynucleotides corresponding to SEQ ID NO:X. Chromosomal location was determined by finding exact matches to EST and cDNA sequences contained in the NCBI (National Center for Biotechnology Information) UniGene database. Given a presumptive chromosomal location, disease locus association was determined by comparison with the Morbid Map, derived from Online Mendelian Inheritance in Man (Online Mendelian Inheritance in Man, OMIM™. McKusick-Nathans Institute for Genetic Medicine, Johns Hopkins University (Baltimore, Md.) and National Center for Biotechnology Information, National Library of Medicine (Bethesda, Md.) 2000. World Wide Web URL: www.ncbi.nlm.nih.gov/omim/). If the putative chromosomal location of the Query overlaps with the chromosomal location of a Morbid Map entry, an OMIM identification number is disclosed in Table 1B.1, column 9 labeled “OMIM Disease Reference(s)”. A key to the OMIM reference identification numbers is provided in Table 5.

Table 1B.2

Column 5 of Table 1B.2, “Tissue Distribution” shows the expression profile of tissue, cells, and/or cell line libraries which express the polynucleotides of the invention. The first code number shown in Table 1B.2 column 5 (preceding the colon), represents the tissue/cell source identifier code corresponding to the key provided in Table 4. Expression of these polynucleotides was not observed in the other tissues and/or cell libraries tested. The second number in column 5 (following the colon), represents the number of times a sequence corresponding to the reference polynucleotide sequence (e.g., SEQ ID NO:X) was identified in the corresponding tissue/cell source. Those tissue/cell source identifier codes in which the first two letters are “AR” designate information generated using DNA array technology. Utilizing this technology, cDNAs were amplified by PCR and then transferred, in duplicate, onto the array. Gene expression was assayed through hybridization of first strand cDNA probes to the DNA array. cDNA probes were generated from total RNA extracted from a variety of different tissues and cell lines. Probe synthesis was performed in the presence of ³³P dCTP, using oligo(dT) to prime reverse transcription. After hybridization, high stringency washing conditions were employed to remove non-specific hybrids from the array. The remaining signal, emanating from each gene target, was measured using a Phosphorimager. Gene expression was reported as Phosphor Stimulating Luminescence (PSL) which reflects the level of phosphor signal generated from the probe hybridized to each of the gene targets represented on the array. A local background signal subtraction was performed before the total signal generated from each array was used to normalize gene expression between the different hybridizations. The value presented after “[array code]:” represents the mean of the duplicate values, following background subtraction and probe normalization. One of skill in the art could routinely use this information to identify normal and/or diseased tissue(s) which show a predominant expression pattern of the corresponding polynucleotide of the invention or to identify polynucleotides which show predominant and/or specific tissue and/or cell expression.

Description of Table 1C

Table 1C summarizes additional polynucleotides encompassed by the invention (including cDNA clones related to the sequences (Clone ID:), contig sequences (contig identifier (Contig ID:) contig nucleotide sequence identifiers (SEQ ID NO:X)), and genomic sequences (SEQ ID NO:B). The first column provides a unique clone identifier, “Clone ID:”, for a cDNA clone related to each contig sequence. The second column provides the sequence identifier, “SEQ ID NO:X”, for each contig sequence. The third column provides a unique contig identifier, “Contig ID:” for each contig sequence. The fourth column, provides a BAC identifier “BAC ID NO:A” for the BAC clone referenced in the corresponding row of the table. The fifth column provides the nucleotide sequence identifier, “SEQ ID NO:B” for a fragment of the BAC clone identified in column four of the corresponding row of the table. The sixth column, “Exon From-To”, provides the location (i.e., nucleotide position numbers) within the polynucleotide sequence of SEQ ID NO:B which delineate certain polynucleotides of the invention that are also exemplary members of polynucleotide sequences that encode polypeptides of the invention (e.g., polypeptides containing amino acid sequences encoded by the polynucleotide sequences delineated in column six, and fragments and variants thereof).

Description of Table 1D

Table 1D: In preferred embodiments, the present invention encompasses a method of detecting, preventing, diagnosing, prognosticating, treating, and/or ameliorating cancer and other hyperproliferative disorders; comprising administering to a patient in which such treatment, prevention, or amelioration is desired a protein, nucleic acid, or antibody of the invention (or fragment or variant thereof) represented by Table 1A, Table 1B, and Table 1C, in an amount effective to detect, prevent, diagnose, prognosticate, treat, and/or ameliorate the disease or disorder.

As indicated in Table 1D, the polynucleotides, polypeptides, agonists, or antagonists of the present invention (including antibodies) can be used in assays to test for one or more biological activities. If these polynucleotides and polypeptides do exhibit activity in a particular assay, it is likely that these molecules may be involved in the diseases associated with the biological activity. Thus, the polynucleotides or polypeptides, or agonists or antagonists thereof (including antibodies) could be used to treat the associated disease.

Table 1D provides information related to biological activities for polynucleotides and polypeptides of the invention (including antibodies, agonists, and/or antagonists thereof). Table 1D also provides information related to assays which may be used to test polynucleotides and polypeptides of the invention (including antibodies, agonists, and/or antagonists thereof) for the corresponding biological activities. The first column (“Gene No.”) provides the gene number in the application for each clone identifier. The second column (“cDNA Clone ID:”) provides the unique clone identifier for each clone as previously described and indicated in Tables 1A, 1B, and 1C. The third column (“AA SEQ ID NO:Y”) indicates the Sequence Listing SEQ ID Number for polypeptide sequences encoded by the corresponding cDNA clones (also as indicated in Tables 1A, 1B, and 2). The fourth column (“Biological Activity”) indicates a biological activity corresponding to the indicated polypeptides (or polynucleotides encoding said polypeptides). The fifth column (“Exemplary Activity Assay”) further describes the corresponding biological activity and provides information pertaining to the various types of assays which may be performed to test, demonstrate, or quantify the corresponding biological activity. Table 1D describes the use of FMAT technology, inter alia, for testing or demonstrating various biological activities. Fluorometric microvolume assay technology (FMAT) is a fluorescence-based system which provides a means to perform nonradioactive cell- and bead-based assays to detect activation of cell signal transduction pathways. This technology was designed specifically for ligand binding and immunological assays. Using this technology, fluorescent cells or beads at the bottom of the well are detected as localized areas of concentrated fluorescence using a data processing system. Unbound fluorophore comprising the background signal is ignored, allowing for a wide variety of homogeneous assays. FMAT technology may be used for peptide ligand binding assays, immunofluorescence, apoptosis, cytotoxicity, and bead-based immunocapture assays. See, Miraglia S et. al., “Homogeneous cell and bead based assays for highthroughput screening using fluorometric microvolume assay technology,” Journal of Biomolecular Screening; 4:193-204 (1999). In particular, FMAT technology may be used to test, confirm, and/or identify the ability of polypeptides (including polypeptide fragments and variants) to activate signal transduction pathways. For example, FMAT technology may be used to test, confirm, and/or identify the ability of polypeptides to upregulate production of immunomodulatory proteins (such as, for example, interleukins, GM-CSF, Rantes, and Tumor Necrosis factors, as well as other cellular regulators (e.g. insulin)).

Table 1D also describes the use of kinase assays for testing, demonstrating, or quantifying biological activity. In this regard, the phosphorylation and de-phosphorylation of specific amino acid residues (e.g. Tyrosine, Serine, Threonine) on cell-signal transduction proteins provides a fast, reversible means for activation and de-activation of cellular signal transduction pathways. Moreover, cell signal transduction via phosphorylation/de-phosphorylation is crucial to the regulation of a wide variety of cellular processes (e.g. proliferation, differentiation, migration, apoptosis, etc.). Accordingly, kinase assays provide a powerful tool useful for testing, confirming, and/or identifying polypeptides (including polypeptide fragments and variants) that mediate cell signal transduction events via protein phosphorylation. See e.g., Forrer, P., Tamaskovic R., and Jaussi, R. “Enzyme-Linked Immunosorbent Assay for Measurement of JNK, ERK, and p38 Kinase Activities” Biol. Chem. 379(8-9): 1101-1110 (1998).

Description of Table 1E

Polynucleotides encoding polypeptides of the present invention can be used in assays to test for one or more biological activities. One such biological activity which may be tested includes the ability of polynucleotides and polypeptides of the invention to stimulate up-regulation or down-regulation of expression of particular genes and proteins. Hence, if polynucleotides and polypeptides of the present invention exhibit activity in altering particular gene and protein expression patterns, it is likely that these polynucleotides and polypeptides of the present invention may be involved in, or capable of effecting changes in, diseases associated with the altered gene and protein expression profiles. Hence, polynucleotides, polypeptides, or antibodies of the present invention could be used to treat said associated diseases.

TaqMan® assays may be performed to assess the ability of polynucleotides (and polypeptides they encode) to alter the expression pattern of particular “target” genes. TaqMan® reactions are performed to evaluate the ability of a test agent to induce or repress expression of specific genes in different cell types. TaqMan® gene expression quantification assays (“TaqMan® assays”) are well known to, and routinely performed by, those of ordinary skill in the art. TaqMan® assays are performed in a two step reverse transcription/polymerase chain reaction (RT-PCR). In the first (RT) step, cDNA is reverse transcribed from total RNA samples using random hexamer primers. In the second (PCR) step, PCR products are synthesized from the cDNA using gene specific primers.

To quantify gene expression the Taqman® PCR reaction exploits the 5′ nuclease activity of AmpliTaq Gold® DNA Polymerase to cleave a Taqman® probe (distinct from the primers) during PCR. The Taqman® probe contains a reporter dye at the 5′-end of the probe and a quencher dye at the 3′ end of the probe. When the probe is intact, the proximity of the reporter dye to the quencher dye results in suppression of the reporter fluorescence. During PCR, if the target of interest is present, the probe specifically anneals between the forward and reverse primer sites. AmpliTaq Fold DNA Polymerase then cleaves the probe between the reporter and quencher when the probe hybridizes to the target, resulting in increased fluorescence of the reporter (see FIG. 2). Accumulation of PCR products is detected directly by monitoring the increase in fluorescence of the reporter dye.

After the probe fragments are displaced from the target, polymerization of the strand continues. The 3′-end of the probe is blocked to prevent extension of the probe during PCR. This process occurs in every cycle and does not interfere with the exponential accumulation of product. The increase in fluorescence signal is detected only if the target sequence is complementary to the probe and is amplified during PCR. Because of these requirements, any nonspecific amplification is not detected.

For test sample preparation, vector controls or constructs containing the coding sequence for the gene of interest are transfected into cells, such as for example 293T cells, and supernatants collected after 48 hours. For cell treatment and RNA isolation, multiple primary human cells or human cell lines are used; such cells may include but are not limited to, Normal Human Dermal Fibroblasts, Aortic Smooth Muscle, Human Umbilical Vein Endothelial Cells, HepG2, Daudi, Jurkat, U937, Caco, and THP-1 cell lines. Cells are plated in growth media and growth is arrested by culturing without media change for 3 days, or by switching cells to low serum media and incubating overnight. Cells are treated for 1, 6, or 24 hours with either vector control supernatant or sample supernatant (or purified/partially purified protein preparations in buffer). Total RNA is isolated; for example, by using TRIZOL™ extraction or by using the Ambion RNAqueous™-4PCR RNA isolation system. Expression levels of multiple genes are analyzed using TAQMAN, and expression in the test sample is compared to control vector samples to identify genes induced or repressed. Each of the above described techniques are well known to, and routinely performed by, those of ordinary skill in the art.

Table 1E indicates particular disease classes and preferred indications for which polynucleotides, polypeptides, or antibodies of the present invention may be used in detecting, diagnosing, preventing, treating and/or ameliorating said diseases and disorders based on “target” gene expression patterns which may be up- or down-regulated by polynucleotides (and the encoded polypeptides) corresponding to each indicated cDNA Clone ID (shown in Table 1E, Column 2).

Thus, in preferred embodiments, the present invention encompasses a method of detecting, diagnosing, preventing, treating, and/or ameliorating a disease or disorder listed in the “Disease Class” and/or “Preferred Indication” columns of Table 1E; comprising administering to a patient in which such detection, diagnosis, prevention, or treatment is desired a protein, nucleic acid, or antibody of the invention (or fragment or variant thereof) in an amount effective to detect, diagnose, prevent, treat, or ameliorate the disease or disorder. The first and second columns of Table 1D show the “Gene No.” and “cDNA Clone ID No.”, respectively, indicating certain nucleic acids and proteins (or antibodies against the same) of the invention (including polynucleotide, polypeptide, and antibody fragments or variants thereof) that may be used in detecting, diagnosing, preventing, treating, or ameliorating the disease(s) or disorder(s) indicated in column 6 and as indicated in the corresponding row in the “Disease Class” or “Preferred Indication” Columns of Table 1E.

In another embodiment, the present invention also encompasses methods of detecting, diagnosing, preventing, treating, or ameliorating a disease or disorder listed in the “Disease Class” or “Preferred Indication” Columns of Table 1E; comprising administering to a patient combinations of the proteins, nucleic acids, or antibodies of the invention (or fragments or variants thereof), sharing similar indications as shown in the corresponding rows in the “Disease Class” or “Preferred Indication” Columns of Table 1E.

The “Disease Class” Column of Table 1E provides a categorized descriptive heading for diseases, disorders, and/or conditions (more fully described below) that may be detected, diagnosed, prevented, treated, or ameliorated by a protein, nucleic acid, or antibody of the invention (or fragment or variant thereof).

The “Preferred Indication” Column of Table 1E describes diseases, disorders, and/or conditions that may be detected, diagnosed, prevented, treated, or ameliorated by a protein, nucleic acid, or antibody of the invention (or fragment or variant thereof).

The “Cell Line” and “Exemplary Targets” Columns of Table 1E indicate particular cell lines and target genes, respectively, which may show altered gene expression patterns (i.e., up- or down-regulation of the indicated target gene) in Taqman assays, performed as described above, utilizing polynucleotides of the cDNA Clone ID shown in the corresponding row. Alteration of expression patterns of the indicated “Exemplary Target” genes is correlated with a particular “Disease Class” and/or “Preferred Indication” as shown in the corresponding row under the respective column headings.

The “Exemplary Accessions” Column indicates GenBank Accessions (available online through the National Center for Biotechnology Information (CBI) at www.ncbi.nlm.nih.gov/) which correspond to the “Exemplary Targets” shown in the adjacent row.

The recitation of “Cancer” in the “Disease Class” Column indicates that the corresponding nucleic acid and protein, or antibody against the same, of the invention (or fragment or variant thereof) may be used for example, to detect, diagnose, prevent, treat, and/or ameliorate neoplastic diseases and/or disorders (e.g., leukemias, cancers, etc., as described below under “Hyperproliferative Disorders”).

The recitation of “Immune” in the “Disease Class” column indicates that the corresponding nucleic acid and protein, or antibody against the same, of the invention (or fragment or variant thereof), may be used for example, to detect, diagnose, prevent, treat, and/or ameliorate diseases and/or disorders relating to neoplastic diseases (e.g., as described below under “Hyperproliferative Disorders”), blood disorders (e.g., as described below under “Immune Activity” “Cardiovascular Disorders” and/or “Blood-Related Disorders”), and infections (e.g., as described below under “Infectious Disease”).

The recitation of “Angiogenesis” in the “Disease Class” column indicates that the corresponding nucleic acid and protein, or antibody against the same, of the invention (or fragment or variant thereof), may be used for example, to detect, diagnose, treat, prevent, and/or ameliorate diseases and/or disorders relating to neoplastic diseases (e.g., as described below under “Hyperproliferative Disorders”), diseases and/or disorders of the cardiovascular system (e.g., as described below under “Cardiovascular Disorders”), diseases and/or disorders involving cellular and genetic abnormalities (e.g., as described below under “Diseases at the Cellular Level”), diseases and/or disorders involving angiogenesis (e.g., as described below under “Anti-Angiogenesis Activity”), to promote or inhibit cell or tissue regeneration (e.g., as described below under “Regeneration”), or to promote wound healing (e.g., as described below under “Wound Healing and Epithelial Cell Proliferation”).

The recitation of “Diabetes” in the “Disease Class” column indicates that the corresponding nucleic acid and protein, or antibody against the same, of the invention (or fragment or variant thereof), may be used for example, to detect, diagnose, treat, prevent, and/or ameliorate diabetes (including diabetes mellitus types I and II), as well as diseases and/or disorders associated with, or consequential to, diabetes (e.g. as described below under “Endocrine Disorders,” “Renal Disorders,” and “Gastrointestinal Disorders”).

Description of Table 2

Table 2 summarizes homology and features of some of the polypeptides of the invention. The first column provides a unique clone identifier, “Clone ID:”, corresponding to a cDNA clone disclosed in Table 1A or Table 1B. The second column provides the unique contig identifier, “Contig ID:” corresponding to contigs in Table 1B and allowing for correlation with the information in Table 1B. The third column provides the sequence identifier, “SEQ ID NO:X”, for the contig polynucleotide sequence. The fourth column provides the analysis method by which the homology/identity disclosed in the Table was determined. Comparisons were made between polypeptides encoded by the polynucleotides of the invention and either a non-redundant protein database (herein referred to as “NR”), or a database of protein families (herein referred to as “PFAM”) as further described below. The fifth column provides a description of the PFAM/NR hit having a significant match to a polypeptide of the invention. Column six provides the accession number of the PFAM/NR hit disclosed in the fifth column. Column seven, “Score/Percent Identity”, provides a quality score or the percent identity, of the hit disclosed in columns five and six. Columns 8 and 9, “NT From” and “NT To” respectively, delineate the polynucleotides in “SEQ ID NO:X” that encode a polypeptide having a significant match to the PFAM/NR database as disclosed in the fifth and sixth columns. In specific embodiments polypeptides of the invention comprise, or alternatively consist of, an amino acid sequence encoded by a polynucleotide in SEQ ID NO:X as delineated in columns 8 and 9, or fragments or variants thereof.

Description of Table 3

Table 3 provides polynucleotide sequences that may be disclaimed according to certain embodiments of the invention. The first column provides a unique clone identifier, “Clone ID”, for a cDNA clone related to contig sequences disclosed in Table 1B. The second column provides the sequence identifier, “SEQ ID NO:X”, for contig sequences disclosed in Table 1A and/or Table 1B. The third column provides the unique contig identifier, “Contig ID:”, for contigs disclosed in Table 1B. The fourth column provides a unique integer ‘a’ where ‘a’ is any integer between 1 and the final nucleotide minus 15 of SEQ ID NO:X, and the fifth column provides a unique integer ‘b’ where ‘b’ is any integer between 15 and the final nucleotide of SEQ ID NO:X, where both a and b correspond to the positions of nucleotide residues shown in SEQ ID NO:X, and where b is greater than or equal to a +14. For each of the polynucleotides shown as SEQ ID NO:X, the uniquely defined integers can be substituted into the general formula of a-b, and used to describe polynucleotides which may be preferably excluded from the invention. In certain embodiments, preferably excluded from the invention are at least one, two, three, four, five, ten, or more of the polynucleotide sequence(s) having the accession number(s) disclosed in the sixth column of this Table (including for example, published sequence in connection with a particular BAC clone). In further embodiments, preferably excluded from the invention are the specific polynucleotide sequence(s) contained in the clones corresponding to at least one, two, three, four, five, ten, or more of the available material having the accession numbers identified in the sixth column of this Table (including for example, the actual sequence contained in an identified BAC clone).

Description of Table 4

Table 4 provides a key to the tissue/cell source identifier code disclosed in Table 1B.2, column 5. Column 1 of Table 4 provides the tissue/cell source identifier code disclosed in Table 1B.2, Column 5. Columns 2-5 provide a description of the tissue or cell source. Note that “Description” and “Tissue” sources (i.e. columns 2 and 3) having the prefix “a_” indicates organs, tissues, or cells derived from “adult” sources. Codes corresponding to diseased tissues are indicated in column 6 with the word “disease.” The use of the word “disease” in column 6 is non-limiting. The tissue or cell source may be specific (e.g. a neoplasm), or may be disease-associated (e.g., a tissue sample from a normal portion of a diseased organ). Furthermore, tissues and/or cells lacking the “disease” designation may still be derived from sources directly or indirectly involved in a disease state or disorder, and therefore may have a further utility in that disease state or disorder. In numerous cases where the tissue/cell source is a library, column 7 identifies the vector used to generate the library.

Description of Table 5

Table 5 provides a key to the OMIM reference identification numbers disclosed in Table 1B.1, column 9. OMIM reference identification numbers (Column 1) were derived from Online Mendelian Inheritance in Man (Online Mendelian Inheritance in Man, OMIM. McKusick-Nathans Institute for Genetic Medicine, Johns Hopkins University (Baltimore, Md.) and National Center for Biotechnology Information, National Library of Medicine, (Bethesda, Md.) 2000. World Wide Web URL: www.ncbi.nlm.nih.gov/omim/). Column 2 provides diseases associated with the cytologic band disclosed in Table 1B.1, column 8, as determined using the Morbid Map database.

Description of Table 6

Table 6 summarizes some of the ATCC™ Deposits, Deposit dates, and ATCC™ designation numbers of deposits made with the ATCC™ in connection with the present application. These deposits were made in addition to those described in the Table 1A.

Description of Table 7

Table 7 shows the cDNA libraries sequenced, and ATCC™ designation numbers and vector information relating to these cDNA libraries.

The first column shows the first four letters indicating the Library from which each library clone was derived. The second column indicates the catalogued tissue description for the corresponding libraries. The third column indicates the vector containing the corresponding clones. The fourth column shows the ATCC™ deposit designation for each library clone as indicated by the deposit information in Table 6.

Definitions

The following definitions are provided to facilitate understanding of certain terms used throughout this specification.

In the present invention, “isolated” refers to material removed from its original environment (e.g., the natural environment if it is naturally occurring), and thus is altered “by the hand of man” from its natural state. For example, an isolated polynucleotide could be part of a vector or a composition of matter, or could be contained within a cell, and still be “isolated” because that vector, composition of matter, or particular cell is not the original environment of the polynucleotide. The term “isolated” does not refer to genomic or cDNA libraries, whole cell total or mRNA preparations, genomic DNA preparations (including those separated by electrophoresis and transferred onto blots), sheared whole cell genomic DNA preparations or other compositions where the art demonstrates no distinguishing features of the polynucleotide/sequences of the present invention.

In the present invention, a “secreted” protein refers to those proteins capable of being directed to the ER, secretory vesicles, or the extracellular space as a result of a signal sequence, as well as those proteins released into the extracellular space without necessarily containing a signal sequence. If the secreted protein is released into the extracellular space, the secreted protein can undergo extracellular processing to produce a “mature” protein. Release into the extracellular space can occur by many mechanisms, including exocytosis and proteolytic cleavage.

As used herein, a “polynucleotide” refers to a molecule having a nucleic acid sequence encoding SEQ ID NO:Y or a fragment or variant thereof (e.g., the polypeptide delinated in columns fourteen and fifteen of Table 1A); a nucleic acid sequence contained in SEQ ID NO:X (as described in column 5 of Table 1A and/or column 3 of Table 1B) or the complement thereof; a cDNA sequence contained in Clone ID: (as described in column 2 of Table 1A and/or Table 1B and contained within a library deposited with the ATCC™); a nucleotide sequence encoding the polypeptide encoded by a nucleotide sequence in SEQ ID NO:B as defined in column 6 (EXON From-To) of Table 1C or a fragment or variant thereof, or a nucleotide coding sequence in SEQ ID NO:B as defined in column 6 of Table 1C or the complement thereof. For example, the polynucleotide can contain the nucleotide sequence of the full length cDNA sequence, including the 5′ and 3′ untranslated sequences, the coding region, as well as fragments, epitopes, domains, and variants of the nucleic acid sequence. Moreover, as used herein, a “polypeptide” refers to a molecule having an amino acid sequence encoded by a polynucleotide of the invention as broadly defined (obviously excluding poly-Phenylalanine or poly-Lysine peptide sequences which result from translation of a polyA tail of a sequence corresponding to a cDNA).

In the present invention, “SEQ ID NO:X” was often generated by overlapping sequences contained in multiple clones (contig analysis). A representative clone containing all or most of the sequence for SEQ ID NO:X is deposited at Human Genome Sciences, Inc. (HGS) in a catalogued and archived library. As shown, for example, in column 2 of Table 1B, each clone is identified by a cDNA Clone ID (identifier generally referred to herein as Clone ID:). Each Clone ID is unique to an individual clone and the Clone ID is all the information needed to retrieve a given clone from the HGS library. Table 7 provides a list of the deposited cDNA libraries. One can use the Clone ID: to determine the library source by reference to Tables 6 and 7. Table 7 lists the deposited cDNA libraries by name and links each library to an ATCC™ Deposit. Library names contain four characters, for example, “HTWE.” The name of a cDNA clone (Clone ID) isolated from that library begins with the same four characters, for example “HTWEP07”. As mentioned below, Table 1A and/or Table 1B correlates the Clone ID names with SEQ ID NO:X. Thus, starting with an SEQ ID NO:X, one can use Tables 1A, 1B, 6, 7, and 9 to determine the corresponding Clone ID, which library it came from and which ATCC™ deposit the library is contained in. Furthermore, it is possible to retrieve a given cDNA clone from the source library by techniques known in the art and described elsewhere herein. The ATCC™ is located at 10801 University Boulevard, Manassas, Va. 20110-2209, USA. The ATCC™ deposits were made pursuant to the terms of the Budapest Treaty on the international recognition of the deposit of microorganisms for the purposes of patent procedure.

In specific embodiments, the polynucleotides of the invention are at least 15, at least 30, at least 50, at least 100, at least 125, at least 500, or at least 1000 continuous nucleotides but are less than or equal to 300 kb, 200 kb, 100 kb, 50 kb, 15 kb, 10 kb, 7.5 kb, 5 kb, 2.5 kb, 2.0 kb, or 1 kb, in length. In a further embodiment, polynucleotides of the invention comprise a portion of the coding sequences, as disclosed herein, but do not comprise all or a portion of any intron. In another embodiment, the polynucleotides comprising coding sequences do not contain coding sequences of a genomic flanking gene (i.e., 5′ or 3′ to the gene of interest in the genome). In other embodiments, the polynucleotides of the invention do not contain the coding sequence of more than 1000, 500, 250, 100, 50, 25, 20, 15, 10, 5, 4, 3, 2, or 1 genomic flanking gene(s).

A “polynucleotide” of the present invention also includes those polynucleotides capable of hybridizing, under stringent hybridization conditions, to sequences contained in SEQ ID NO:X, or the complement thereof (e.g., the complement of any one, two, three, four, or more of the polynucleotide fragments described herein), the polynucleotide sequence delineated in columns 7 and 8 of Table 1A or the complement thereof, the polynucleotide sequence delineated in columns 8 and 9 of Table 2 or the complement thereof, and/or cDNA sequences contained in Clone ID: (e.g., the complement of any one, two, three, four, or more of the polynucleotide fragments, or the cDNA clone within the pool of cDNA clones deposited with the ATCC™, described herein), and/or the polynucleotide sequence delineated in column 6 of Table 1C or the complement thereof. “Stringent hybridization conditions” refers to an overnight incubation at 42 degree C. in a solution comprising 50% formamide, 5×SSC (750 mM NaCl, 75 mM trisodium citrate), 50 mM sodium phosphate (pH 7.6), 5×Denhardt's solution, 10% dextran sulfate, and 20 μg/ml denatured, sheared salmon sperm DNA, followed by washing the filters in 0.1×SSC at about 65 degree C.

Also contemplated are nucleic acid molecules that hybridize to the polynucleotides of the present invention at lower stringency hybridization conditions. Changes in the stringency of hybridization and signal detection are primarily accomplished through the manipulation of formamide concentration (lower percentages of formamide result in lowered stringency); salt conditions, or temperature. For example, lower stringency conditions include an overnight incubation at 37 degree C. in a solution comprising 6×SSPE (20×SSPE=3M NaCl; 0.2M NaH₂PO₄; 0.02M EDTA, pH 7.4), 0.5% SDS, 30% formamide, 100 ug/ml salmon sperm blocking DNA; followed by washes at 50 degree C. with 1×SSPE, 0.1% SDS. In addition, to achieve even lower stringency, washes performed following stringent hybridization can be done at higher salt concentrations (e.g. 5×SSC).

Note that variations in the above conditions may be accomplished through the inclusion and/or substitution of alternate blocking reagents used to suppress background in hybridization experiments. Typical blocking reagents include Denhardt's reagent, BLOTTO, heparin, denatured salmon sperm DNA, and commercially available proprietary formulations. The inclusion of specific blocking reagents may require modification of the hybridization conditions described above, due to problems with compatibility.

Of course, a polynucleotide which hybridizes only to polyA+ sequences (such as any 3′ terminal polyA+ tract of a cDNA shown in the sequence listing), or to a complementary stretch of T (or U) residues, would not be included in the definition of “polynucleotide,” since such a polynucleotide would hybridize to any nucleic acid molecule containing a poly (A) stretch or the complement thereof (e.g., practically any double-stranded cDNA clone generated using oligo dT as a primer).

The polynucleotide of the present invention can be composed of any polyribonucleotide or polydeoxyribonucleotide, which may be unmodified RNA or DNA or modified RNA or DNA. For example, polynucleotides can be composed of single- and double-stranded DNA, DNA that is a mixture of single- and double-stranded regions, single- and double-stranded RNA, and RNA that is mixture of single- and double-stranded regions, hybrid molecules comprising DNA and RNA that may be single-stranded or, more typically, double-stranded or a mixture of single- and double-stranded regions. In addition, the polynucleotide can be composed of triple-stranded regions comprising RNA or DNA or both RNA and DNA. A polynucleotide may also contain one or more modified bases or DNA or RNA backbones modified for stability or for other reasons. “Modified” bases include, for example, tritylated bases and unusual bases such as inosine. A variety of modifications can be made to DNA and RNA; thus, “polynucleotide” embraces chemically, enzymatically, or metabolically modified forms.

In specific embodiments, the polynucleotides of the invention are at least 15, at least 30, at least 50, at least 100, at least 125, at least 500, or at least 1000 continuous nucleotides but are less than or equal to 300 kb, 200 kb, 100 kb, 50 kb, 15 kb, 10 kb, 7.5 kb, 5 kb, 2.5 kb, 2.0 kb, or 1 kb, in length. In a further embodiment, polynucleotides of the invention comprise a portion of the coding sequences, as disclosed herein, but do not comprise all or a portion of any intron. In another embodiment, the polynucleotides comprising coding sequences do not contain coding sequences of a genomic flanking gene (i.e., 5′ or 3′ to the gene of interest in the genome). In other embodiments, the polynucleotides of the invention do not contain the coding sequence of more than 1000, 500, 250, 100, 50, 25, 20, 15, 10, 5, 4, 3, 2, or 1 genomic flanking gene(s).

“SEQ ID NO:X” refers to a polynucleotide sequence described in column 5 of Table 1A, while “SEQ ID NO:Y” refers to a polypeptide sequence described in column 10 of Table 1A. SEQ ID NO:X is identified by an integer specified in column 6 of Table 1A. The polypeptide sequence SEQ ID NO:Y is a translated open reading frame (ORF) encoded by polynucleotide SEQ ID NO:X. The polynucleotide sequences are shown in the sequence listing immediately followed by all of the polypeptide sequences. Thus, a polypeptide sequence corresponding to polynucleotide sequence SEQ ID NO:2 is the first polypeptide sequence shown in the sequence listing. The second polypeptide sequence corresponds to the polynucleotide sequence shown as SEQ ID NO:3, and so on.

The polypeptide of the present invention can be composed of amino acids joined to each other by peptide bonds or modified peptide bonds, i.e., peptide isosteres, and may contain amino acids other than the 20 gene-encoded amino acids. The polypeptides may be modified by either natural processes, such as posttranslational processing, or by chemical modification techniques which are well known in the art. Such modifications are well described in basic texts and in more detailed monographs, as well as in a voluminous research literature. Modifications can occur anywhere in a polypeptide, including the peptide backbone, the amino acid side-chains and the amino or carboxyl termini. It will be appreciated that the same type of modification may be present in the same or varying degrees at several sites in a given polypeptide. Also, a given polypeptide may contain many types of modifications. Polypeptides may be branched, for example, as a result of ubiquitination, and they may be cyclic, with or without branching. Cyclic, branched, and branched cyclic polypeptides may result from posttranslation natural processes or may be made by synthetic methods. Modifications include acetylation, acylation, ADP-ribosylation, amidation, covalent attachment of flavin, covalent attachment of a heme moiety, covalent attachment of a nucleotide or nucleotide derivative, covalent attachment of a lipid or lipid derivative, covalent attachment of phosphotidylinositol, cross-linking, cyclization, disulfide bond formation, demethylation, formation of covalent cross-links, formation of cysteine, formation of pyroglutamate, formylation, gamma-carboxylation, glycosylation, GPI anchor formation, hydroxylation, iodination, methylation, myristoylation, oxidation, pegylation, proteolytic processing, phosphorylation, prenylation, racemization, selenoylation, sulfation, transfer-RNA mediated addition of amino acids to proteins such as arginylation, and ubiquitination. (See, for instance, PROTEINS—STRUCTURE AND MOLECULAR PROPERTIES, 2nd Ed., T. E. Creighton, W. H. Freeman and Company, New York (1993); POSTTRANSLATIONAL COVALENT MODIFICATION OF PROTEINS, B. C. Johnson, Ed., Academic Press, New York, pgs. 1-12 (1983); Seifter et al., Meth. Enzymol. 182:626-646 (1990); Rattan et al., Ann. N.Y. Acad. Sci. 663:48-62 (1992)).

“SEQ ID NO:X” refers to a polynucleotide sequence described, for example, in Tables 1A, Table 1B, or Table 2, while “SEQ ID NO:Y” refers to a polypeptide sequence described in column 11 of Table 1A and or column 6 of Table 1B.I. SEQ ID NO:X is identified by an integer specified in column 4 of Table 1B. The polypeptide sequence SEQ ID NO:Y is a translated open reading frame (ORF) encoded by polynucleotide SEQ ID NO:X. “Clone ID:” refers to a cDNA clone described in column 2 of Table 1A and/or 1B.

“A polypeptide having functional activity” refers to a polypeptide capable of displaying one or more known functional activities associated with a full-length (complete) protein. Such functional activities include, but are not limited to, biological activity (e.g. activity useful in treating, preventing and/or ameliorating cancer and other hyperproliferative disorders), antigenicity (ability to bind [or compete with a polypeptide for binding] to an anti-polypeptide antibody), immunogenicity (ability to generate antibody which binds to a specific polypeptide of the invention), ability to form multimers with polypeptides of the invention, and ability to bind to a receptor or ligand for a polypeptide.

The polypeptides of the invention can be assayed for functional activity (e.g. biological activity) using or routinely modifying assays known in the art, as well as assays described herein. Specifically, one of skill in the art may routinely assay secreted polypeptides (including fragments and variants) of the invention for activity using assays as described in the examples section below.

“A polypeptide having biological activity” refers to a polypeptide exhibiting activity similar to, but not necessarily identical to, an activity of a polypeptide of the present invention, including mature forms, as measured in a particular biological assay, with or without dose dependency. In the case where dose dependency does exist, it need not be identical to that of the polypeptide, but rather substantially similar to the dose-dependence in a given activity as compared to the polypeptide of the present invention (i.e., the candidate polypeptide will exhibit greater activity or not more than about 25-fold less and, preferably, not more than about tenfold less activity, and most preferably, not more than about three-fold less activity relative to the polypeptide of the present invention).

Tables:

Table 1A

Table 1A summarizes information concerning certain polynucleotides and polypeptides of the invention. The first column provides the gene number in the application for each clone identifier. The second column provides a unique clone identifier, “Clone ID:”, for a cDNA clone related to each contig sequence disclosed in Table 1A. Third column, the cDNA Clones identified in the second column were deposited as indicated in the third column (i.e. by ATCC™ Deposit No:Z and deposit date). Some of the deposits contain multiple different clones corresponding to the same gene. In the fourth column, “Vector” refers to the type of vector contained in the corresponding cDNA Clone identified in the second column. In the fifth column, the nucleotide sequence identified as “NT SEQ ID NO:X” was assembled from partially homologous (“overlapping”) sequences obtained from the corresponding cDNA clone identified in the second column and, in some cases, from additional related cDNA clones. The overlapping sequences were assembled into a single contiguous sequence of high redundancy (usually three to five overlapping sequences at each nucleotide position), resulting in a final sequence identified as SEQ ID NO:X. In the sixth column, “Total NT Seq.” refers to the total number of nucleotides in the contig sequence identified as SEQ ID NO:X.” The deposited clone may contain all or most of these sequences, reflected by the nucleotide position indicated as “5′ NT of Clone Seq.” (seventh column) and the “3′ NT of Clone Seq.” (eighth column) of SEQ ID NO:X. In the ninth column, the nucleotide position of SEQ ID NO:X of the putative start codon (methionine) is identified as “5′ NT of Start Codon.” Similarly, in column ten, the nucleotide position of SEQ ID NO:X of the predicted signal sequence is identified as “5′ NT of First AA of Signal Pep.” In the eleventh column, the translated amino acid sequence, beginning with the methionine, is identified as “AA SEQ ID NO:Y,” although other reading frames can also be routinely translated using known molecular biology techniques. The polypeptides produced by these alternative open reading frames are specifically contemplated by the present invention.

In the twelfth and thirteenth columns of Table 1A, the first and last amino acid position of SEQ ID NO:Y of the predicted signal peptide is identified as “First AA of Sig Pep” and “Last AA of Sig Pep.” In the fourteenth column, the predicted first amino acid position of SEQ ID NO:Y of the secreted portion is identified as “Predicted First AA of Secreted Portion”. The amino acid position of SEQ ID NO:Y of the last amino acid encoded by the open reading frame is identified in the fifteenth column as “Last AA of ORF”.

SEQ ID NO:X (where X may be any of the polynucleotide sequences disclosed in the sequence listing) and the translated SEQ ID NO:Y (where Y may be any of the polypeptide sequences disclosed in the sequence listing) are sufficiently accurate and otherwise suitable for a variety of uses well known in the art and described further below. For instance, SEQ ID NO:X is useful for designing nucleic acid hybridization probes that will detect nucleic acid sequences contained in SEQ ID NO:X or the cDNA contained in the deposited clone. These probes will also hybridize to nucleic acid molecules in biological samples, thereby enabling a variety of forensic and diagnostic methods of the invention. Similarly, polypeptides identified from SEQ ID NO:Y may be used, for example, to generate antibodies which bind specifically to proteins containing the polypeptides and the secreted proteins encoded by the cDNA clones identified in Table 1A and/or elsewhere herein

Nevertheless, DNA sequences generated by sequencing reactions can contain sequencing errors. The errors exist as misidentified nucleotides, or as insertions or deletions of nucleotides in the generated DNA sequence. The erroneously inserted or deleted nucleotides cause frame shifts in the reading frames of the predicted amino acid sequence. In these cases, the predicted amino acid sequence diverges from the actual amino acid sequence, even though the generated DNA sequence may be greater than 99.9% identical to the actual DNA sequence (for example, one base insertion or deletion in an open reading frame of over 1000 bases).

Accordingly, for those applications requiring precision in the nucleotide sequence or the amino acid sequence, the present invention provides not only the generated nucleotide sequence identified as SEQ ID NO:X, and the predicted translated amino acid sequence identified as SEQ ID NO:Y, but also a sample of plasmid DNA containing a human cDNA of the invention deposited with the ATCC™, as set forth in Table 1A. The nucleotide sequence of each deposited plasmid can readily be determined by sequencing the deposited plasmid in accordance with known methods

The predicted amino acid sequence can then be verified from such deposits. Moreover, the amino acid sequence of the protein encoded by a particular plasmid can also be directly determined by peptide sequencing or by expressing the protein in a suitable host cell containing the deposited human cDNA, collecting the protein, and determining its sequence.

Also provided in Table 1A is the name of the vector which contains the cDNA plasmid. Each vector is routinely used in the art. The following additional information is provided for convenience.

Vectors Lambda Zap (U.S. Pat. Nos. 5,128,256 and 5,286,636), Uni-Zap XR (U.S. Pat. Nos. 5,128,256 and 5,286,636), Zap Express (U.S. Pat. Nos. 5,128,256 and 5,286,636), pBLUESCRIPT™ (pBS) (Short, J. M. et al., Nucleic Acids Res. 16:7583-7600 (1988); Alting-Mees, M. A. and Short, J. M., Nucleic Acids Res. 17.9494 (1989)) and pBK (Alting-Mees, M. A. et al., Strategies 5:58-61 (1992)) are commercially available from STRATAGENE™ Cloning Systems, Inc., 11011 N. Torrey Pines Road, La Jolla, Calif., 92037. pBS contains an ampicillin resistance gene and pBK contains a neomycin resistance gene. Phagemid pBS may be excised from the Lambda Zap and Uni-Zap XR vectors, and phagemid pBK may be excised from the Zap Express vector. Both phagemids may be transformed into E. coli strain XL-1 Blue, also available from STRATAGENE™

Vectors pSport1, pCMVSport 1.0, pCMVSport 2.0 and pCMVSport 3.0, were obtained from LIFE TECHNOLOGIES™, Inc., P.O. Box 6009, Gaithersburg, Md. 20897. All Sport vectors contain an ampicillin resistance gene and may be transformed into E. coli strain DH10B, also available from LIFE TECHNOLOGIES™. See, for instance, Gruber, C. E., et al., Focus 15.59 (1993). Vector lafmid BA (Bento Soares, Columbia University, New York, N.Y.) contains an ampicillin resistance gene and can be transformed into E. coli strain XL-1 Blue. Vector pCR®2.1, which is available from Invitrogen, 1600 Faraday Avenue, Carlsbad, Calif. 92008, contains an ampicillin resistance gene and may be transformed into E. coli strain DH10B, available from LIFE TECHNOLOGIES™. See, for instance, Clark, J. M., Nuc. Acids Res. 16:9677-9686 (1988) and Mead, D. et al., Bio/Technology 9: (1991).

The present invention also relates to the genes corresponding to SEQ ID NO:X, SEQ ID NO:Y, and/or a deposited cDNA (cDNA Clone ID). The corresponding gene can be isolated in accordance with known methods using the sequence information disclosed herein. Such methods include, but are not limited to, preparing probes or primers from the disclosed sequence and identifying or amplifying the corresponding gene from appropriate sources of genomic material.

Also provided in the present invention are allelic variants, orthologs, and/or species homologs. Procedures known in the art can be used to obtain full-length genes, allelic variants, splice variants, full-length coding portions, orthologs, and/or species homologs of genes corresponding to SEQ ID NO:X and SEQ ID NO:Y using information from the sequences disclosed herein or the clones deposited with the ATCC™. For example, allelic variants and/or species homologs may be isolated and identified by making suitable probes or primers from the sequences provided herein and screening a suitable nucleic acid source for allelic variants and/or the desired homologue.

The present invention provides a polynucleotide comprising, or alternatively consisting of, the nucleic acid sequence of SEQ ID NO:X and/or a cDNA contained in ATCC™ Deposit No.Z. The present invention also provides a polypeptide comprising, or alternatively, consisting of, the polypeptide sequence of SEQ ID NO:Y, a polypeptide encoded by SEQ ID NO:X, and/or a polypeptide encoded by a cDNA contained in ATCC™ deposit No.Z. Polynucleotides encoding a polypeptide comprising, or alternatively consisting of the polypeptide sequence of SEQ ID NO:Y, a polypeptide encoded by SEQ ID NO:X and/or a polypeptide encoded by the cDNA contained in ATCC™ Deposit No.Z, are also encompassed by the invention. The present invention further encompasses a polynucleotide comprising, or alternatively consisting of the complement of the nucleic acid sequence of SEQ ID NO:X, and/or the complement of the coding strand of the cDNA contained in ATCC™ Deposit No.Z. TABLE 1A First NT 5′ NT 5′ NT AA First Last AA SEQ 5′ NT 3′ NT of of First SEQ AA AA of Last ID Total of of Start AA of ID of of Secret- AA Gene cDNA Clone ATCC ™ Deposit NO: NT Clone Clone Co- Signal NO: Sig Sig ed of No. ID No: Z and Date Vector X Seq. Seq. Seq. don Pep Y Pep Pep Portion ORF 1 H2CBG48 209889 May 22, 1998 pBLUESCRIPT ™ 11 2797 1 2797 125 125 949 1 25 26 45 SK− 2 H2MAC30 209299 Sep. 25, 1997 pBLUESCRIPT ™ 12 459 1 459 157 157 950 1 28 29 72 SK− 3 H6EAB28 209511 Dec. 03, 1997 Uni-ZAP XR 13 1939 1 1939 115 115 951 1 31 32 100 3 H6EAB28 209511 Dec. 03, 1997 Uni-ZAP XR 631 1547 1 1547 116 116 1570 1 20 21 76 4 H6EDF66 209299 Sep. 25, 1997 Uni-ZAP XR 14 540 1 540 146 146 952 1 27 28 131 5 HABAG37 209626 Feb. 12, 1998 pSport1 15 654 1 639 97 97 953 1 31 32 62 6 HACBD91 209626 Feb. 12, 1998 Uni-ZAP XR 16 1445 1 1445 117 117 954 1 42 43 49 7 HACCI17 203071 Jul. 27, 1998 Uni-ZAP XR 17 1722 336 1714 461 461 955 1 24 25 218 7 HACCI17 203071 Jul. 27, 1998 Uni-ZAP XR 633 1380 12 1380 135 135 1572 1 24 25 72 8 HADAO89 209423 Oct. 30, 1997 pSport1 18 1453 1 1453 244 244 956 1 22 23 44 9 HAGAI85 97922 Mar. 07, 1997 Uni-ZAP XR 19 1752 52 1752 166 166 957 1 23 24 30 209070 May 22, 1997 10 HAGAM64 209603 Jan. 29, 1998 Uni-ZAP XR 20 2321 1 2321 57 57 958 1 31 32 44 11 HAGAN21 PTA-841 Uni-ZAP XR 21 843 1 843 34 34 959 1 17 18 91 Oct. 13, 1999 11 HAGAN21 PTA-841 Uni-ZAP XR 634 610 294 610 335 335 1572 1 17 18 91 Oct. 13, 1999 11 HAGAN21 PTA-841 Uni-ZAP XR 635 659 1 659 452 1573 1 4 Oct. 13, 1999 11 HAGAN21 PTA-841 Uni-ZAP XR 636 189 1 189 146 1574 1 13 14 14 Oct. 13, 1999 11 HAGAN21 PTA-841 Uni-ZAP XR 637 637 1 637 321 1575 1 6 Oct. 13, 1999 12 HAGBZ81 209118 Jun. 12, 1997 Uni-ZAP XR 22 1382 24 1382 65 960 1 30 31 49 13 HAGDG59 209277 Sep. 18, 1997 Uni-ZAP XR 23 1734 44 1717 124 124 961 1 18 19 300 14 HAGDI35 209852 May 07, 1998 Uni-ZAP XR 24 1357 1 1338 318 318 962 1 25 26 93 15 HAGFG51 203364 Oct. 19, 1998 Uni-ZAP XR 25 1313 1 1313 163 163 163 1 23 24 43 16 HAGFI62 209782 Apr. 20, 1998 Uni-ZAP XR 26 1003 368 992 429 429 964 1 28 29 91 17 HAGFY16 97923 Mar. 07, 1997 Uni-ZAP XR 27 1963 209 1922 251 251 965 1 28 29 198 209071 May 22, 1997 17 HAGFY16 97923 Mar. 07, 1997 Uni-ZAP XR 638 1830 87 1786 128 128 1576 1 26 27 45 209071 May 22, 1997 18 HAHDB16 209626 Feb. 12, 1998 Uni-ZAP XR 28 796 1 796 93 93 966 1 20 21 50 19 HAHDR32 209626 Feb. 12, 1998 Uni-ZAP XR 29 1256 365 1256 435 435 967 1 25 26 181 20 HAIBO71 209145 Jul. 17, 1997 Uni-ZAP XR 30 752 172 752 325 325 968 1 28 29 66 21 HAIBP89 209877 May 18, 1998 Uni-ZAP XR 31 2243 173 2243 311 311 969 1 27 28 317 21 HAIBP89 209877 May 18, 1998 Uni-ZAP XR 639 1025 1 1025 1 1577 1 1 2 18 22 HAICP19 209009 Apr. 28, 1997 Uni-ZAP XR 32 1624 89 1483 128 128 970 1 18 19 446 23 HAIFL18 209852 May 07, 1998 Uni-ZAP XR 33 879 1 879 274 274 971 1 29 30 140 24 HAJAF57 203364 Oct. 19, 1998 pCMVSport 3.0 34 2761 1 2761 43 43 972 1 1 2 94 25 HAJBR69 209626 Feb. 12, 1998 pCMVSport 3.0 35 755 1 755 262 262 973 1 19 20 53 26 HAJBZ75 209603 Jan. 29, 1998 pCMVSport 3.0 36 2089 10 2085 49 49 974 1 22 23 607 27 HAMFK58 209641 Feb. 25, 1998 pCMVSport 3.0 37 785 1 785 279 279 975 1 31 32 79 28 HAMGG68 209878 May 18, 1998 pCMVSport 3.0 38 1458 1 1458 312 312 976 1 20 21 55 29 HANGG89 PTA-1543 pSport1 39 2657 348 2398 520 520 977 1 1 2 52 Mar. 21, 2000 29 HANGG89 PTA-1543 pSport1 640 2454 1 2454 125 125 1578 1 23 24 98 Mar. 21, 2000 29 HANGG89 PTA-1543 pSport1 641 1775 1 1775 70 70 1579 1 29 30 392 Mar. 21, 2000 29 HANGG89 PTA-1543 pSport1 642 1379 1 1379 78 78 1580 1 26 27 434 Mar. 21, 2000 30 HAPBS03 209651 Mar. 04, 1998 Uni-ZAP XR 40 1503 45 1479 252 252 978 1 28 29 41 31 HAPNY86 209511 Dec. 03, 1997 Uni-ZAP XR 41 1280 1 1280 100 100 979 1 25 26 129 32 HAPNY94 209889 May 22, 1998 Uni-ZAP XR 42 742 1 742 94 94 980 1 29 30 50 33 HAPPW30 209683 Mar. 20, 1998 Uni-ZAP XR 43 1472 1 1472 59 59 981 1 22 23 264 33 HAPPW30 209683 Mar. 20, 1998 Uni-ZAP XR 643 1508 14 1501 54 54 1580 1 22 23 91 34 HAPQT22 203070 Jul. 27, 1998 Uni-ZAP XR 44 635 1 635 132 132 982 1 17 18 72 35 HAPUC89 203570 Jan. 11, 1999 Uni-ZAP XR 45 1153 1 1153 385 385 983 1 25 26 140 36 HASAV70 97923 Mar. 07, 1997 Uni-ZAP XR 46 729 1 729 94 94 984 1 20 21 110 209071 May 22, 1997 36 HASAV70 97923 Mar. 07, 1997 Uni-ZAP XR 644 1412 10 733 103 103 1582 1 20 21 110 209071 May 22, 1997 37 HASCG84 209568 Jan. 06, 1998 Uni-ZAP XR 47 1079 1 1079 216 216 985 1 32 33 53 38 HATAC53 209651 Mar. 04, 1998 Uni-ZAP XR 48 1959 1 1959 97 97 986 1 21 22 248 38 HATAC53 209651 Mar. 04, 1998 Uni-ZAP XR 645 1306 13 1306 99 99 1583 1 21 22 189 39 HATBR65 209626 Feb. 12, 1998 Uni-ZAP XR 49 812 1 812 252 252 987 1 16 17 64 40 HATCB92 209683 Mar. 20, 1998 Uni-ZAP XR 50 1756 1 1756 247 247 988 1 37 38 56 41 HATCP77 209965 Jun. 11, 1998 Uni-ZAP XR 51 2098 1 2098 37 37 989 1 21 22 182 42 HATEE46 209407 Oct. 23, 1997 Uni-ZAP XR 52 1675 136 863 241 241 990 1 21 22 53 43 HBAFJ33 209603 Jan. 29, 1998 pSport1 53 1280 1 1252 60 60 991 1 15 16 110 44 HBAFV19 PTA-1543 pSport1 54 953 1 953 6 6 992 1 1 2 258 Mar. 21, 2000 45 HBAMB34 209324 Oct. 02, 1997 pSport1 55 1027 1 1027 87 87 993 1 35 36 48 46 HBCPB32 PTA-2075 pSport1 56 1368 1 1368 88 88 994 1 37 38 202 Jun. 09, 2000 46 HBCPB32 PTA-2075 pSport1 646 729 1 729 89 89 1584 1 37 38 196 Jun. 09, 2000 47 HBCQL32 PTA-2075 pSport1 57 402 1 402 26 26 995 1 20 21 80 Jun. 09, 2000 47 HBCQL32 PTA-2075 pSport1 647 1180 741 1180 760 760 1585 1 20 21 80 Jun. 09, 2000 48 HBGNU56 PTA-2073 Uni-ZAP XR 58 864 1 864 125 125 996 1 21 22 185 Jun. 09, 2000 48 HBGNU56 PTA-2073 Uni-ZAP XR 648 941 1 941 79 79 1586 1 21 22 178 Jun. 09, 2000 48 HBGNU56 PTA-2073 Uni-ZAP XR 649 988 804 853 2 1587 1 1 2 219 Jun. 09, 2000 49 HBHAD12 209009 Apr. 28, 1997 Uni-ZAP XR 59 786 1 786 176 997 1 17 18 23 50 HBHMA23 209782 Apr. 20, 1998 pSport1 60 1175 2 1175 71 71 998 1 24 25 197 50 HBHMA23 209782 Apr. 20, 1998 pSport1 650 1172 1 1172 70 70 1588 1 24 25 76 51 HBIMB51 209683 Mar. 20, 1998 pCMVSport 3.0 61 537 1 537 98 98 999 1 21 22 146 51 HBIMB51 209683 Mar. 20, 1998 pCMVSport 3.0 651 526 1 526 93 93 1589 1 21 22 130 52 HBINS58 PTA-885 pCMVSport 3.0 62 843 1 843 57 57 1000 1 30 31 174 Oct. 28, 1999 52 HBINS58 PTA-885 pCMVSport 3.0 652 1566 1 1566 71 71 1590 1 29 30 173 Oct. 28, 1999 52 HBINS58 PTA-885 pCMVSport 3.0 653 1067 1 1067 100 100 1591 1 29 30 210 Oct. 28, 1999 53 HBJFU48 209125 Jun. 19, 1997 Uni-ZAP XR 63 849 1 849 20 20 1001 1 39 40 40 54 HBJIY92 203071 Jul. 27, 1998 Uni-ZAP XR 64 2434 487 2366 548 548 1002 1 29 30 40 55 HBJLC01 209651 Mar. 04, 1998 Uni-ZAP XR 65 872 1 872 87 87 1003 1 34 35 46 56 HBJLF01 209877 May 18, 1998 Uni-ZAP XR 66 1932 201 1931 217 217 1004 1 46 47 244 57 HBJLH40 203499 Dec. 01, 1998 Uni-ZAP XR 67 1853 1 1853 74 74 1005 1 30 31 74 58 HBJNC59 PTA-622 Uni-ZAP XR 68 1061 1 1061 66 66 1006 1 22 23 245 Sep. 02, 1999 58 HBJNC59 PTA-622 Uni-ZAP XR 654 1021 1 1021 66 66 1592 1 22 23 99 Sep. 02, 1999 58 HBJNC59 PTA-622 Uni-ZAP XR 655 1086 1 1023 64 64 1593 1 22 23 245 Sep. 02, 1999 59 HBMCI50 97978 Mar. 27, 1997 pBLUESCRIPT ™ 69 920 1 920 156 156 1007 1 29 30 83 209075 May 22, 1997 60 HBNAW17 209242 Sep. 12, 1997 Uni-ZAP XR 70 601 1 601 77 77 1008 1 37 38 61 61 HBOEG11 PTA-2072 pSport1 71 1356 1 1356 57 57 1009 1 22 23 250 Jun. 09, 2000 61 HBOEG11 PTA-2072 pSport1 656 1352 1 1352 53 53 1594 1 22 23 250 Jun. 09, 2000 61 HBOEG11 PTA-2072 pSport1 657 1337 1 1289 47 47 1595 1 22 23 250 Jun. 09, 2000 62 HBOEG69 203081 Jul. 30, 1998 pSport1 72 1411 1 1411 302 302 1010 1 19 20 54 63 HBXFL29 203858 Mar. 18, 1999 ZAP Express 73 2229 376 2210 560 560 1011 1 31 32 57 64 HCACU58 209626 Feb. 12, 1998 Uni-ZAP XR 74 1554 1 1554 137 137 1012 1 30 31 83 65 HCACV51 209551 Dec. 12, 1997 Uni-ZAP XR 75 2083 1 2083 168 168 1013 1 31 32 81 65 HCACV51 209551 Dec. 12, 1997 Uni-ZAP XR 658 2092 1 2092 173 173 1596 1 31 32 281 66 HCDAF84 209300 Sep. 25, 1997 Uni-ZAP XR 76 427 1 427 168 168 1014 1 18 19 56 67 HCE1Q89 209242 Sep. 12, 1997 Uni-ZAP XR 77 863 1 863 74 74 1015 1 17 18 88 68 HCE2F54 209626 Feb. 12, 1998 Uni-ZAP XR 78 1276 19 1256 166 166 1016 1 19 20 319 69 HCEFB80 PTA-2069 Uni-ZAP XR 79 2494 1 2494 12 12 1017 1 35 36 89 Jun. 09, 2000 69 HCEFB80 PTA-2069 Uni-ZAP XR 659 2494 1 2451 5 5 1597 1 35 36 89 Jun. 09, 2000 70 HCEGR33 209090 Jun. 05, 1997 Uni-ZAP XR 80 1630 1 1630 243 243 1018 1 18 19 31 71 HCEMP62 209745 Apr. 07, 1998 Uni-ZAP XR 81 1860 269 1726 352 352 1019 1 30 31 187 71 HCEMP62 209745 Apr. 07, 1998 Uni-ZAP XR 660 1957 582 1823 19 19 1598 1 33 34 335 72 HCENK38 209651 Mar. 04, 1998 Uni-ZAP XR 82 1509 1 1509 10 10 1020 1 28 29 52 73 HCEWE17 PTA-842 Uni-ZAP XR 83 967 1 967 117 117 1021 1 23 24 106 Oct. 13, 1999 73 HCEWE17 PTA-842 Uni-ZAP XR 661 730 247 730 500 500 1599 1 19 20 27 Oct. 13, 1999 73 HCEWE17 PTA-842 Uni-ZAP XR 662 550 1 550 156 1600 1 1 2 54 Oct. 13, 1999 74 HCEWE20 209300 Sep. 25, 1997 Uni-ZAP XR 84 885 13 885 166 166 1022 1 18 19 51 75 HCFCU88 209324 Oct. 02, 1997 pSport1 85 853 1 853 217 217 1023 1 18 19 97 76 HCFMV71 209242 Sep. 12, 1997 pSport1 86 400 1 400 31 31 1024 1 24 25 58 77 HCFNN01 209086 May 29, 1997 pSport1 87 1261 154 1261 254 254 1025 1 27 28 43 78 HCFOM18 209324 Oct. 02, 1997 pSport1 88 639 1 639 28 28 1026 1 20 21 63 79 HCHNF25 209651 Mar. 04, 1998 pSport1 89 3576 1 3576 1130 1130 1027 1 30 31 169 79 HCHNF25 209651 Mar. 04, 1998 pSport1 663 807 1 807 180 180 1601 1 30 31 147 80 HCMSQ56 209877 May 18, 1998 Uni-ZAP XR 90 1262 1 1262 148 148 1028 1 19 20 88 81 HCMST14 209346 Oct. 09, 1997 Uni-ZAP XR 91 614 1 614 136 136 1029 1 24 25 47 82 HCMTB45 209368 Oct. 16, 1997 Uni-ZAP XR 92 958 1 958 215 215 1030 1 20 21 123 82 HCMTB45 209368 Oct. 16, 1997 Uni-ZAP XR 664 946 1 946 209 209 1602 1 27 28 70 83 HCNSB61 209242 Sep. 12, 1997 pBLUESCRIPT ™ 93 712 1 712 218 218 1031 1 21 22 43 84 HCNSD93 209627 Feb. 12, 1998 pBLUESCRIPT ™ 94 1106 1 1106 139 139 1032 1 21 22 46 85 HCNSM70 209580 Jan. 14, 1998 pBLUESCRIPT ™ 95 1089 1 1089 107 107 1033 1 26 27 215 85 HCNSM70 209580 Jan. 14, 1998 pBLUESCRIPT ™ 665 1145 62 1145 161 161 1603 1 26 27 91 86 HCOOS80 PTA-2076 pSport1 96 1254 1 1254 36 36 1034 1 26 27 158 Jun. 09, 2000 86 HCOOS80 PTA-2076 pSport1 666 869 15 869 40 40 1604 1 26 27 158 Jun. 09, 2000 86 HCOOS80 PTA-2076 pSport1 667 692 339 506 1 1605 1 1 2 106 Jun. 09, 2000 87 HCUBS50 209215 Aug. 21, 1997 ZAP Express 97 865 1 865 88 88 1035 1 34 35 38 88 HCUCK44 209853 May 07, 1998 ZAP Express 98 1139 573 1133 593 593 1036 1 30 31 60 89 HCUEO60 209215 Aug. 21, 1997 ZAP Express 99 1222 1 1222 102 102 1037 1 34 35 64 90 HCUHK65 209641 Feb. 25, 1998 ZAP Express 100 367 1 367 80 80 1038 1 26 27 79 90 HCUHK65 209641 Feb. 25, 1998 ZAP Express 668 3113 2577 2946 770 770 1606 1 30 31 708 91 HCUIM65 209324 Oct. 02, 1997 ZAP Express 101 875 331 736 557 557 1039 1 27 28 47 92 HCWEB58 PTA-883 ZAP Express 102 1283 1 1283 148 148 1040 1 27 28 343 Oct. 28, 1999 92 HCWEB58 PTA-883 ZAP Express 669 980 1 980 247 247 1607 1 27 28 244 Oct. 28, 1999 92 HCWEB58 PTA-883 ZAP Express 670 888 1 888 155 155 1608 1 27 28 244 Oct. 28, 1999 93 HCWGU37 PTA-883 ZAP Express 103 2777 1 2777 194 194 1041 1 10 Oct. 28, 1999 93 HCWGU37 PTA-883 ZAP Express 671 1651 1 1651 187 187 1609 1 10 Oct. 28, 1999 94 HCWKC15 209324 Oct. 02, 1997 ZAP Express 104 710 1 710 37 37 1042 1 18 19 40 95 HCWLD74 209626 Feb. 12, 1998 ZAP Express 105 1540 1 1540 138 138 1043 1 21 22 65 96 HCWUM50 209627 Feb. 12, 1998 ZAP Express 106 1428 208 1428 270 270 1044 1 30 31 45 97 HCYBG92 209563 Dec. 18, 1997 pBLUESCRIPT ™ 107 3061 1 2661 118 118 1045 1 21 22 274 SK− 98 HDABR72 209965 Jun. 11, 1998 pSport1 108 1691 1 1691 33 33 1046 1 29 30 146 98 HDABR72 209965 Jun. 11, 1998 pSport1 672 1746 1 1746 28 28 1610 1 29 30 146 99 HDHEB60 209215 Aug. 21, 1997 pCMVSport 2.0 109 1421 235 1421 568 568 1047 1 24 25 108 100 HDHIA94 209627 Feb. 12, 1998 pCMVSport 2.0 110 1489 1 1489 154 154 1048 1 30 31 168 100 HDHIA94 209627 Feb. 12, 1998 pCMVSport 2.0 673 2492 1 2492 163 163 1611 1 30 31 48 101 HDHMA72 209324 Oct. 02, 1997 pCMVSport 2.0 111 4463 216 2158 287 287 1049 1 36 37 315 102 HDLAC10 209745 Apr. 07, 1998 pCMVSport 2.0 112 1477 1 1477 132 132 1050 1 29 30 81 103 HDLAO28 PTA-499 pCMVSport 2.0 113 1984 1 1984 259 259 1051 1 21 22 76 Aug. 11, 1999 104 HDPBI32 209853 May 07, 1998 pCMVSport 3.0 114 1513 1 1513 37 37 1052 1 315 316 316 104 HDPBI32 209853 May 07, 1998 pCMVSport 3.0 674 1579 598 1184 103 103 1612 1 30 31 271 104 HDPBI32 209853 May 07, 1998 pCMVSport 3.0 675 587 1 587 51 51 1613 1 35 36 138 105 HDPBQ71 209877 May 18, 1998 pCMVSport 3.0 115 2312 1 2312 93 93 1053 1 33 34 612 105 HDPBQ71 209877 May 18, 1998 pCMVSport 3.0 676 2242 6 2242 24 24 1614 1 33 34 612 105 HDPBQ71 209877 May 18, 1998 pCMVSport 3.0 677 2381 146 2381 165 165 1615 1 33 34 456 106 HDPCJ91 209877 May 18, 1998 pCMVSport 3.0 116 6107 1 6107 131 131 1054 1 28 29 51 107 HDPCO25 209125 Jun. 19, 1997 pCMVSport 3.0 117 767 76 767 182 182 1055 1 20 21 53 108 HDPCY37 209568 Jan. 06, 1998 pCMVSport 3.0 118 1932 45 1932 76 76 1056 1 21 22 578 108 HDPCY37 209568 Jan. 06, 1998 pCMVSport 3.0 678 1931 45 1931 76 76 1616 1 21 22 264 109 HDPFB02 PTA-622 pCMVSport 3.0 119 3436 1 3436 173 173 1057 1 19 20 152 Sep. 02, 1999 109 HDPFB02 PTA-622 pCMVSport 3.0 679 1517 1 1517 139 139 1617 1 28 29 316 Sep. 02, 1999 109 HDPFB02 PTA-622 pCMVSport 3.0 680 2751 1976 2751 218 218 1618 1 18 19 302 Sep. 02, 1999 110 HDPFF39 209511 Dec. 03, 1997 pCMVSport 3.0 120 1256 1 1256 175 175 1058 1 18 19 196 111 HDPFP29 209626 Feb. 12, 1998 pCMVSport 3.0 121 1057 1 1057 293 293 1059 1 30 31 52 112 HDPGI49 203070 Jul. 27, 1998 pCMVSport 3.0 122 2683 1 2640 266 266 1060 1 29 30 72 113 HDPGP94 203364 Oct. 19, 1998 pCMVSport 3.0 123 3881 1 3881 256 256 1061 1 18 19 74 114 HDPHI51 209125 Jun. 19, 1997 pCMVSport 3.0 124 728 1 728 245 245 1062 1 30 31 40 115 HDPJF37 209852 May 07, 1998 pCMVSport 3.0 125 986 1 986 196 196 1063 1 23 24 57 116 HDPMM88 PTA-848 pCMVSport 3.0 126 4893 1 4893 100 100 1064 1 37 38 937 Oct. 13, 1999 116 HDPMM88 PTA-848 pCMVSport 3.0 681 468 1 468 141 141 1619 1 20 21 109 Oct. 13, 1999 116 HDPMM88 PTA-848 pCMVSport 3.0 682 181 1 181 44 1620 1 7 8 46 Oct. 13, 1999 116 HDPMM88 PTA-848 pCMVSport 3.0 683 612 1 612 419 1621 1 6 Oct. 13, 1999 116 HDPMM88 PTA-848 pCMVSport 3.0 684 1024 1 1024 111 1622 1 5 6 11 Oct. 13, 1999 116 HDPMM88 PTA-848 pCMVSport 3.0 685 366 18 321 167 1623 1 1 2 56 Oct. 13, 1999 116 HDPMM88 PTA-848 pCMVSport 3.0 686 519 1 519 28 1624 1 1 2 53 Oct. 13, 1999 117 HDPNC61 209627 Feb. 12, 1998 pCMVSport 3.0 127 1410 1 1410 20 20 1065 1 22 23 94 118 HDPND46 209627 Feb. 12, 1998 pCMVSport 3.0 128 1727 1 1727 15 15 1066 1 22 23 484 119 HDPOE32 PTA-622 pCMVSport 3.0 129 1353 1 1353 118 118 1067 1 34 35 151 Sep. 02, 1999 120 HDPOH06 209745 Apr. 07, 1998 pCMVSport 3.0 130 2504 1 2504 252 252 1068 1 29 30 242 121 HDPOZ56 209889 May 22, 1998 pCMVSport 3.0 131 1905 1 1905 91 91 1069 1 21 22 567 121 HDPOZ56 209889 May 22, 1998 pCMVSport 3.0 687 1867 415 1867 103 103 1625 1 21 22 566 121 HDPOZ56 209889 May 22, 1998 pCMVSport 3.0 688 1722 1 1722 59 59 1626 1 21 22 319 122 HDPSP54 209782 Apr. 20, 1998 pCMVSport 3.0 132 3091 2304 3091 2356 2356 1070 1 18 19 48 122 HDPSP54 209782 Apr. 20, 1998 pCMVSport 3.0 689 536 1 536 179 179 1627 1 41 42 55 123 HDPTD15 209782 Apr. 20, 1998 pCMVSport 3.0 133 1396 1 1396 223 223 1071 1 18 19 200 124 HDPTK41 209965 Jun. 11, 1998 pCMVSport 3.0 134 1564 1 1564 39 39 1072 1 26 27 369 125 HDPUG50 209745 Apr. 07, 1998 pCMVSport 3.0 135 1734 1 1734 22 22 1073 1 34 35 526 126 HDPUH26 PTA-163 pCMVSport 3.0 136 2916 1 2916 90 90 1074 1 18 19 549 Jun. 01, 1999 127 HDPUW68 203331 Oct. 08, 1998 pCMVSport 3.0 137 1748 1 1748 40 40 1075 1 18 19 467 128 HDPVH60 203105 Aug. 13, 1998 pCMVSport 3.0 138 3116 1 3100 8 8 1076 1 45 46 51 129 HDPVW11 PTA-869 pCMVSport 3.0 139 2339 1 2339 67 67 1077 1 28 29 455 Oct. 26, 1999 129 HDPVW11 PTA-869 pCMVSport 3.0 690 397 1 397 50 50 1628 1 28 29 99 Oct. 26, 1999 130 HDPWN93 PTA-868 pCMVSport 3.0 140 2679 1 2669 45 45 1078 1 19 20 802 Oct. 26, 1999 130 HDPWN93 PTA-868 pCMVSport 3.0 691 716 1 716 35 35 1629 1 19 20 214 Oct. 26, 1999 130 HDPWN93 PTA-868 pCMVSport 3.0 692 2716 26 2716 27 27 1630 1 19 20 43 Oct. 26, 1999 131 HDPWU34 209782 Apr. 20, 1998 pCMVSport 3.0 141 1277 860 1277 117 117 1079 1 23 24 325 131 HDPWU34 209782 Apr. 20, 1998 pCMVSport 3.0 693 427 1 427 111 111 1631 1 16 17 44 132 HDQHD03 203570 Jan. 11, 1999 pCMVSport 3.0 142 1266 1 1266 274 274 1080 1 20 21 331 132 HDQHD03 203570 Jan. 11, 1999 pCMVSport 3.0 694 1257 1 1257 259 259 1632 1 20 21 333 133 HDTBD53 PTA-848 pCMVSport 2.0 143 2803 1 2803 288 288 1081 1 22 23 365 Oct. 13, 1999 133 HDTBD53 PTA-848 pCMVSport 2.0 695 3302 1 2718 292 292 1633 1 22 23 365 Oct. 13, 1999 134 HDTBP04 209300 Sep. 25, 1997 pCMVSport 2.0 144 961 1 961 70 70 1082 1 15 16 219 134 HDTBP04 209300 Sep. 25, 1997 pCMVSport 2.0 696 959 1 959 65 65 1634 1 15 16 220 135 HDTDQ23 209965 Jun. 11, 1998 pCMVSport 2.0 145 2207 1 2207 132 132 1083 1 20 21 56 135 HDTDQ23 209965 Jun. 11, 1998 pCMVSport 2.0 697 2227 1 2206 148 148 1635 1 20 21 108 135 HDTDQ23 209965 Jun. 11, 1998 pCMVSport 2.0 698 2214 1 2206 148 148 1636 1 20 21 73 136 HDTEK44 PTA-867 pCMVSport 2.0 146 2070 20 2070 691 1084 1 12 13 83 Oct. 26, 1999 136 HDTEK44 PTA-867 pCMVSport 2.0 699 1005 1 1005 175 175 1637 1 17 18 67 Oct. 26, 1999 136 HDTEK44 PTA-867 pCMVSport 2.0 700 2988 1 2988 116 116 1638 1 17 18 67 Oct. 26, 1999 136 HDTEK44 PTA-867 pCMVSport 2.0 701 2052 2 2052 673 1639 1 12 13 83 Oct. 26, 1999 137 HDTEN81 209463 Nov. 14, 1997 pCMVSport 2.0 147 566 1 566 114 114 1085 1 17 18 85 138 HDTFE17 PTA-868 pCMVSport 2.0 148 1242 1 1242 260 260 1086 1 20 21 29 Oct. 26, 1999 138 HDTFE17 PTA-868 pCMVSport 2.0 702 628 1 628 251 251 1640 1 20 21 29 Oct. 26, 1999 138 HDTFE17 PTA-868 pCMVSport 2.0 703 923 29 903 101 1641 1 6 7 80 Oct. 26, 1999 139 HDTGC73 209627 Feb. 12, 1998 pCMVSport 2.0 149 712 1 712 386 386 1087 1 31 32 49 140 HDTIT10 203570 Jan. 11, 1999 pCMVSport 2.0 150 1200 1 813 58 58 1088 1 56 57 297 140 HDTIT10 203570 Jan. 11, 1999 pCMVSport 2.0 704 1159 1 805 161 161 1642 1 30 31 56 141 HDTMK50 PTA-884 pCMVSport 2.0 151 1352 1 1352 154 154 1089 1 21 22 51 Oct. 28, 1999 141 HDTMK50 PTA-884 pCMVSport 2.0 705 912 1 912 164 164 1643 1 21 22 51 Oct. 28, 1999 141 HDTMK50 PTA-884 pCMVSport 2.0 706 321 1 321 200 1644 1 1 Oct. 28, 1999 142 HE2DY70 209877 May 18, 1998 Uni-ZAP XR 152 639 1 639 137 137 1090 1 45 46 58 143 HE2EB74 209225 Aug. 28, 1997 Uni-ZAP XR 153 1434 311 1418 507 507 1091 1 15 16 19 144 HE2EN04 209300 Sep. 25, 1997 Uni-ZAP XR 154 370 1 370 57 57 1092 1 16 17 50 145 HE2FV03 97955 Mar. 13, 1997 Uni-ZAP XR 155 2067 1 1251 116 116 1093 1 21 22 42 209074 May 22, 1997 146 HE2NV57 209877 May 18, 1998 Uni-ZAP XR 156 867 1 867 99 99 1094 1 36 37 99 147 HE2PD49 209627 Feb. 12, 1998 Uni-ZAP XR 157 1422 257 1404 337 337 1095 1 18 19 171 148 HE2PY40 209965 Jun. 11, 1998 Uni-ZAP XR 158 1288 1 1288 147 147 1096 1 22 23 83 149 HE6EU50 97975 Apr. 04, 1997 Uni-ZAP XR 159 1152 117 686 237 237 1097 1 20 21 34 209081 May 29, 1997 150 HE8DS15 PTA-1544 Uni-ZAP XR 160 2199 1 2199 91 91 1098 1 24 25 72 Mar. 21, 2000 151 HE8MH91 209603 Jan. 29, 1998 Uni-ZAP XR 161 1761 1 1761 63 63 1099 1 23 24 116 152 HE8QV67 PTA-2072 Uni-ZAP XR 162 1999 643 1999 502 502 1100 1 49 50 80 Jun. 09, 2000 152 HE8QV67 PTA-2072 Uni-ZAP XR 707 2342 1956 2276 256 1645 1 1 2 415 Jun. 09, 2000 153 HE9BK23 209683 Mar. 20, 1998 Uni-ZAP XR 163 1636 1 1636 39 39 1101 1 21 22 309 154 HE9CP41 209368 Oct. 16, 1997 Uni-ZAP XR 164 1392 1 1392 132 132 1102 1 20 21 41 155 HE9DG49 97923 Mar. 07, 1997 Uni-ZAP XR 165 717 1 717 70 70 1103 1 28 29 201 209071 May 22, 1997 155 HE9DG49 97923 Mar. 07, 1997 Uni-ZAP XR 708 717 1 717 70 70 1646 1 27 28 201 209071 May 22, 1997 155 HE9DG49 97923 Mar. 07, 1997 Uni-ZAP XR 709 713 17 713 78 78 1647 1 28 29 203 209071 May 22, 1997 156 HE9HY07 209010 Apr. 28, 1997 Uni-ZAP XR 166 832 1 832 35 35 1104 1 26 27 41 209085 May 29, 1997 157 HE9NN84 Uni-ZAP XR 167 734 1 734 380 380 1105 1 38 39 53 158 HE9OW20 203570 Jan. 11, 1999 Uni-ZAP XR 168 1209 1 1209 129 129 1106 1 33 34 355 158 HE9OW20 203570 Jan. 11, 1999 Uni-ZAP XR 710 1165 1 1165 136 136 1648 1 30 31 313 158 HE9OW20 203570 Jan. 11, 1999 Uni-ZAP XR 711 1160 1 1160 129 129 1649 1 30 31 134 159 HE9RM63 PTA-499 Uni-ZAP XR 169 2149 1 2149 82 82 1107 1 27 28 354 Aug. 11, 1999 160 HEAAR07 209346 Oct. 09, 1997 Uni-ZAP XR 170 1084 1 1084 48 48 1108 1 31 32 42 161 HEBAE88 209242 Sep. 12, 1997 Uni-ZAP XR 171 582 1 582 160 160 1109 1 26 27 42 162 HEBBN36 209141 Jul. 09, 1997 Uni-ZAP XR 172 1046 470 1046 645 645 1110 1 29 30 53 163 HEBCM63 209141 Jul. 09, 1997 Uni-ZAP XR 173 558 1 558 246 246 1111 1 26 27 68 164 HEBEJ18 203069 Jul. 27, 1998 Uni-ZAP XR 174 685 7 649 51 51 1112 1 15 16 139 165 HEEAG23 209745 Apr. 07, 1998 Uni-ZAP XR 175 1669 25 1280 57 57 1113 1 18 19 46 166 HEEAJ02 209627 Feb. 12, 1998 Uni-ZAP XR 176 1038 148 1037 387 387 1114 1 40 41 125 167 HEEAQ11 203071 Jul. 27, 1998 Uni-ZAP XR 177 921 1 921 213 213 1115 1 28 29 147 168 HEEBI05 PTA-2076 Uni-ZAP XR 178 894 1 894 146 146 1116 1 22 23 159 Jun. 09, 2000 168 HEEBI05 PTA-2076 Uni-ZAP XR 712 979 88 979 226 226 1650 1 22 23 159 Jun. 09, 2000 169 HEGAH43 209277 Sep. 18, 1997 Uni-ZAP XR 179 442 1 442 29 29 1117 1 20 21 111 170 HEGAN94 203071 Jul. 27, 1998 Uni-ZAP XR 180 582 1 582 52 52 1118 1 23 24 121 170 HEGAN94 203071 Jul. 27, 1998 Uni-ZAP XR 713 680 1 680 133 133 1651 1 23 24 121 171 HEGBS69 PTA-2082 Uni-ZAP XR 181 809 1 809 260 260 1119 1 20 21 161 Jun. 09, 2000 171 HEGBS69 PTA-2082 Uni-ZAP XR 714 1188 1 807 253 253 1652 1 20 21 161 Jun. 09, 2000 172 HELGK31 209878 May 18, 1998 Uni-ZAP XR 182 1396 25 1334 209 209 1120 1 29 30 344 172 HELGK31 209878 May 18, 1998 Uni-ZAP XR 715 1342 68 1342 402 402 1653 1 1 2 291 173 HELHD85 PTA-1544 Uni-ZAP XR 183 1886 1 1886 41 41 1121 1 25 26 79 Mar. 21, 2000 174 HELHL48 209877 May 18, 1998 Uni-ZAP XR 184 2971 560 2557 629 629 1122 1 16 17 291 174 HELHL48 209877 May 18, 1998 Uni-ZAP XR 716 1955 1 1955 31 31 1654 1 16 17 184 175 HEMAM41 209010 Apr. 28, 1997 Uni-ZAP XR 185 1337 60 1328 175 175 1123 1 39 40 190 209085 May 29, 1997 175 HEMAM41 209010 Apr. 28, 1997 Uni-ZAP XR 717 1338 33 1327 175 175 1655 1 32 33 91 209085 May 29, 1997 176 HEPAA46 209551 Dec. 12, 1997 Uni-ZAP XR 186 1129 1 1129 18 18 1124 1 20 21 123 177 HEPAB80 209423 Oct. 30, 1997 Uni-ZAP XR 187 799 1 799 73 73 1125 1 28 29 121 177 HEPAB80 209423 Oct. 30, 1997 Uni-ZAP XR 718 802 1 802 67 67 1656 1 28 29 122 178 HEQAK71 209551 Dec. 12, 1997 pCMVSport 3.0 188 1689 1 1689 198 198 1126 1 17 18 44 179 HERAR44 209407 Oct. 23, 1997 Uni-ZAP XR 189 420 1 420 60 60 1127 1 40 41 45 180 HESAJ10 209242 Sep. 12, 1997 Uni-ZAP XR 190 1090 400 1090 405 405 1128 1 23 24 71 181 HETAB45 209580 Jan. 14, 1998 Uni-ZAP XR 191 1676 1 1676 123 123 1129 1 30 31 179 182 HETBR16 209877 May 18, 1998 Uni-ZAP XR 192 1569 1 1569 161 161 1130 1 21 22 64 183 HETLM70 PTA-2073 Uni-ZAP XR 193 1251 1 1199 336 336 1131 1 27 28 229 Jun. 09, 2000 183 HETLM70 PTA-2073 Uni-ZAP XR 719 1251 1 1251 336 336 1657 1 27 28 229 Jun. 09, 2000 183 HETLM70 PTA-2073 Uni-ZAP XR 720 517 161 517 2 1658 1 1 2 85 Jun. 09, 2000 184 HFABG18 PTA-1544 Uni-ZAP XR 194 1345 1 1345 53 53 1132 1 26 27 87 Mar. 21, 2000 185 HFAMB72 209146 Jul. 17, 1997 Uni-ZAP XR 195 1323 509 1323 559 559 1133 1 22 23 60 186 HFAMH77 209300 Sep. 25, 1997 Uni-ZAP XR 196 669 96 669 240 240 1134 1 33 34 61 187 HFCCQ50 209463 Nov. 14, 1997 Uni-ZAP XR 197 1271 1 1271 47 47 1135 1 20 21 352 188 HFCEW05 209603 Jan. 29, 1998 Uni-ZAP XR 198 933 1 933 34 34 1136 1 18 19 209 189 HFFAD59 209242 Sep. 12, 1997 Lambda ZAP II 199 470 1 470 44 44 1137 1 17 18 45 190 HFFAL36 209368 Oct. 16, 1997 Lambda ZAP II 200 1020 1 1020 68 68 1138 1 35 36 56 191 HFGAD82 209225 Aug. 28, 1997 Uni-ZAP XR 201 1881 772 1861 1019 1019 1139 1 18 19 38 192 HFIIZ70 PTA-846 pSport1 202 1408 1 1408 24 24 1140 1 23 24 47 Oct. 13, 1999 192 HFIIZ70 PTA-846 pSport1 721 1441 43 1441 74 74 1659 1 23 24 47 Oct. 13, 1999 193 HFKET18 PTA-622 Uni-ZAP XR 203 2407 1 2407 137 137 1141 1 14 15 74 Sep. 02, 1999 194 HFKFG02 209627 Feb. 12, 1998 Uni-ZAP XR 204 795 1 795 110 110 1142 1 18 19 53 195 HFOXB13 209423 Oct. 30, 1997 pSport1 205 1169 1 1169 36 36 1143 1 21 22 54 196 HFPAC12 209511 Dec. 03, 1997 Uni-ZAP XR 206 1088 1 1088 140 140 1144 1 21 22 88 197 HFPAO71 209626 Feb. 12, 1998 Uni-ZAP XR 207 2067 364 2067 414 414 1145 1 33 34 131 198 HFPCX09 209551 Dec. 12, 1997 Uni-ZAP XR 208 2213 1 2213 185 185 1146 1 26 27 549 198 HFPCX09 209551 Dec. 12, 1997 Uni-ZAP XR 722 2674 59 2674 249 249 1660 1 26 27 549 198 HFPCX09 209551 Dec. 12, 1997 Uni-ZAP XR 723 2207 1 2207 185 185 1661 1 26 27 66 199 HFPCX36 209242 Sep. 12, 1997 Uni-ZAP XR 209 796 1 796 103 103 1147 1 27 28 46 200 HFRAN90 209242 Sep. 12, 1997 Uni-ZAP XR 210 532 1 532 178 178 1148 1 33 34 54 201 HFTCU19 209119 Jun. 12, 1997 Uni-ZAP XR 211 1575 1266 1575 137 137 1149 1 30 31 222 201 HFTCU19 209119 Jun. 12, 1997 Uni-ZAP XR 724 470 1 470 157 157 1662 1 24 25 56 202 HFTDL56 209782 Apr. 20, 1998 Uni-ZAP XR 212 1839 32 1838 93 93 1150 1 20 21 519 203 HFTDZ36 209300 Sep. 25, 1997 Uni-ZAP XR 213 1103 231 1103 547 547 1151 1 22 23 68 204 HFVAB79 209368 Oct. 16, 1997 Uni-ZAP XR 214 1175 1 1175 133 133 1152 1 15 16 194 204 HFVAB79 209368 Oct. 16, 1997 Uni-ZAP XR 725 1186 1 1186 139 139 1663 1 15 16 194 205 HFVGE32 PTA-844 pBLUESCRIPT ™ 215 572 1 572 154 154 1153 1 32 33 79 Oct. 13, 1999 205 HFVGE32 PTA-844 pBLUESCRIPT ™ 726 470 2 470 1 1664 1 1 2 67 Oct. 13, 1999 206 HFVIC62 203105 Aug. 13, 1998 pBLUESCRIPT ™ 216 1350 1 1350 114 114 1154 1 31 32 56 207 HFXAM76 209568 Jan. 06, 1998 Lambda ZAP II 217 947 1 947 213 213 1155 1 24 25 79 208 HFXDJ75 209603 Jan. 29, 1998 Lambda ZAP II 218 1918 1 1914 44 44 1156 1 26 27 41 209 HFXDN63 209346 Oct. 09, 1997 Lambda ZAP II 219 1026 1 1026 33 33 1157 1 14 15 53 210 HFXGT26 209965 Jun. 11, 1998 Lambda ZAP II 220 1757 1 1757 13 13 1158 1 22 23 85 211 HFXGV31 209242 Sep. 12, 1997 Lambda ZAP II 221 752 1 752 100 100 1159 1 24 25 64 212 HFXHD88 209511 Dec. 03, 1997 Lambda ZAP II 222 1602 1 1602 130 130 1160 1 41 42 128 213 HFXHK73 209580 Jan. 14, 1998 Lambda ZAP II 223 1873 1 1873 247 247 1161 1 36 37 67 214 HFXKJ03 209215 Aug. 21, 1997 Lambda ZAP II 224 941 1 941 179 179 1162 1 33 34 41 215 HFXKT05 209651 Mar. 04, 1998 Lambda ZAP II 225 1715 1 1715 204 204 1163 1 18 19 79 216 HFXKY27 209877 May 18, 1998 Lambda ZAP II 226 945 1 945 44 44 1164 1 19 20 58 217 HGBFO79 209011 Apr. 28, 1997 Uni-ZAP XR 227 1538 259 1538 273 273 1165 1 23 24 49 218 HGBHE57 209407 Oct. 23, 1997 Uni-ZAP XR 228 663 1 663 14 14 1166 1 19 20 68 219 HGBIB74 203648 Feb. 09, 1999 Uni-ZAP XR 229 1816 1 1804 14 14 1167 1 23 24 377 219 HGBIB74 203648 Feb. 09, 1999 Uni-ZAP XR 727 1821 1 1821 28 28 1665 1 20 21 170 219 HGBIB74 203648 Feb. 09, 1999 Uni-ZAP XR 728 1094 1 1094 2 1666 1 1 2 151 220 HGLAL82 209242 Sep. 12, 1997 Uni-ZAP XR 230 406 1 406 144 144 1168 1 19 20 26 221 HHAAF20 203648 Feb. 09, 1999 Uni-ZAP XR 231 1495 1 1495 141 141 1169 1 18 19 55 222 HHBCS39 PTA-848 pCMVSport 1 232 2895 1 2895 104 104 1170 1 26 27 166 Oct. 13, 1999 222 HHBCS39 PTA-848 pCMVSport 1 729 1042 1 1042 150 150 1667 1 26 27 166 Oct. 13, 1999 222 HHBCS39 PTA-848 pCMVSport 1 730 1556 171 1556 1260 1668 1 16 17 26 Oct. 13, 1999 223 HHEAA08 209853 May 07, 1998 pCMVSport 3.0 233 2150 1 2150 88 88 1171 1 38 39 79 223 HHEAA08 209853 May 07, 1998 pCMVSport 3.0 731 615 1 615 311 1669 1 13 14 20 224 HHEMA59 203364 Oct. 19, 1998 pCMVSport 3.0 234 3102 1 3099 239 239 1172 1 20 21 76 225 HHEMA75 209179 Jul. 24, 1997 pCMVSport 3.0 235 865 229 865 569 569 1173 1 35 36 84 226 HHEMM74 PTA-849 pCMVSport 3.0 236 2612 1 2612 94 94 1174 1 27 28 74 Oct. 13, 1999 226 HHEMM74 PTA-849 pCMVSport 3.0 732 1125 1 1125 121 121 1670 1 27 28 74 Oct. 13, 1999 226 HHEMM74 PTA-849 pCMVSport 3.0 733 2297 1425 2297 706 1671 1 6 7 33 Oct. 13, 1999 226 HHEMM74 PTA-849 pCMVSport 3.0 734 482 33 482 7 1672 1 13 14 53 Oct. 13, 1999 227 HHENQ22 209511 Dec. 03, 1997 pCMVSport 3.0 237 1899 1 1899 115 115 1175 1 36 37 58 228 HHEPD24 209195 Aug. 01, 1997 pCMVSport 3.0 238 238 1 238 156 156 1176 1 23 24 27 229 HHEPM33 PTA-322 pCMVSport 3.0 239 1459 1 1459 269 269 1177 1 20 21 82 Jul. 09, 1999 230 HHEPT60 209138 Jul. 03, 1997 pCMVSport 3.0 240 532 21 532 245 245 1178 1 18 19 36 231 HHEPU04 203648 Feb. 09, 1999 pCMVSport 3.0 241 1084 116 1084 259 259 1179 1 31 32 163 231 HHEPU04 203648 Feb. 09, 1999 pCMVSport 3.0 735 1081 124 1081 267 267 1673 1 31 32 163 231 HHEPU04 203648 Feb. 09, 1999 pCMVSport 3.0 736 720 1 720 45 45 1674 1 31 32 92 232 HHFBY53 203364 Oct. 19, 1998 Uni-ZAP XR 242 870 1 870 172 172 1180 1 18 19 64 233 HHFEC49 PTA-844 Uni-ZAP XR 243 2263 1 2263 30 30 1181 1 24 25 184 Oct. 13, 1999 234 HHFFJ48 209627 Feb. 12, 1998 Uni-ZAP XR 244 2566 1 2566 65 65 1182 1 21 22 106 235 HHFGR93 209746 Apr. 07, 1998 Uni-ZAP XR 245 1835 1 1835 132 132 1183 1 29 30 390 235 HHFGR93 209746 Apr. 07, 1998 Uni-ZAP XR 737 1932 1 1836 130 130 1675 1 29 30 236 236 HHFHJ59 97975 Apr. 04, 1997 Uni-ZAP XR 246 661 1 661 192 192 1184 1 29 30 112 209081 May 29, 1997 237 HHFHR32 97975 Apr. 04, 1997 Uni-ZAP XR 247 1378 1 1378 58 58 1185 1 25 26 235 209081 May 29, 1997 238 HHFOJ29 PTA-2075 Uni-ZAP XR 248 1366 1 1366 117 117 1186 1 31 32 82 Jun. 09, 2000 238 HHFOJ29 PTA-2075 Uni-ZAP XR 738 1595 513 1595 132 132 1676 1 19 20 95 Jun. 09, 2000 238 HHFOJ29 PTA-2075 Uni-ZAP XR 739 970 272 970 62 1677 1 1 2 152 Jun. 09, 2000 239 HHGBO91 209242 Sep. 12, 1997 Lambda ZAP II 249 715 1 715 140 140 1187 1 28 29 49 240 HHGCM76 97958 Mar. 13, 1997 Lambda ZAP II 250 711 8 711 270 270 1188 1 22 23 89 209072 May 22, 1997 240 HHGCM76 97958 Mar. 13, 1997 Lambda ZAP II 740 711 8 711 270 270 1678 1 11 209072 May 22, 1997 241 HHGCQ54 209300 Sep. 25, 1997 Lambda ZAP II 251 875 1 875 62 62 1189 1 15 16 51 242 HHGDF16 209463 Nov. 14, 1997 Lambda ZAP II 252 890 215 890 253 253 1190 1 26 27 52 243 HHGDW43 209346 Oct. 09, 1997 Lambda ZAP II 253 1050 1 1050 107 107 1191 1 40 41 44 244 HHPDX20 209580 Jan. 14, 1998 Uni-ZAP XR 254 1161 1 1161 174 174 1192 1 30 31 66 245 HHPGO40 209878 May 18, 1998 Uni-ZAP XR 255 1002 1 1002 116 116 1193 1 26 27 295 245 HHPGO40 209878 May 18, 1998 Uni-ZAP XR 741 973 1 973 68 68 1679 1 37 38 302 245 HHPGO40 209878 May 18, 1998 Uni-ZAP XR 742 984 1 984 74 74 1680 1 37 38 224 246 HHPTJ65 209179 Jul. 24, 1997 Uni-ZAP XR 256 515 1 515 247 247 1194 1 32 33 48 247 HHSDX28 209346 Oct. 09, 1997 Uni-ZAP XR 257 1113 1 1113 90 90 1195 1 21 22 56 248 HILCF66 209627 Feb. 12, 1998 pBLUESCRIPT ™ 258 1668 740 1668 331 331 1196 1 21 22 44 SK− 249 HJACG02 209215 Aug. 21, 1997 pBLUESCRIPT ™ 259 575 1 575 66 66 1197 1 22 23 108 SK− 249 HJACG02 209215 Aug. 21, 1997 pBLUESCRIPT ™ 743 553 1 553 47 47 1681 1 23 24 108 SK− 250 HJACG30 PTA-843 pBLUESCRIPT ™ 260 1532 1 1532 291 291 1198 1 27 28 44 Oct. 13, 1999 SK− 250 HJACG30 PTA-843 pBLUESCRIPT ™ 744 1614 1020 1614 50 1682 1 1 2 130 Oct. 13, 1999 SK− 250 HJACG30 PTA-843 pBLUESCRIPT ™ 745 1087 491 1087 350 1683 1 1 2 122 Oct. 13, 1999 SK− 251 HJBCU04 PTA-322 pBLUESCRIPT ™ 261 1192 1 1192 96 96 1199 1 49 50 176 Jul. 09, 1999 SK− 252 HJBCY35 209877 May 18, 1998 pBLUESCRIPT ™ 262 1559 93 1272 232 232 1200 1 23 24 327 SK− 253 HJMBI18 209580 Jan. 14, 1998 pCMVSport 3.0 263 1021 303 1021 574 574 1201 1 19 20 80 254 HJMBM38 209300 Sep. 25, 1997 pCMVSport 3.0 264 1024 316 1023 387 387 1202 1 14 15 112 255 HJMBT65 209580 Jan. 14, 1998 pCMVSport 3.0 265 621 79 621 341 341 1203 1 33 34 42 256 HJMBW30 209146 Jul. 17, 1997 pCMVSport 3.0 266 884 1 874 110 110 1204 1 18 19 42 257 HJPAD75 209641 Feb. 25, 1998 Uni-ZAP XR 267 1231 1 1231 60 60 1205 1 29 30 91 258 HJPCP42 PTA-843 Uni-ZAP XR 268 1223 1 1223 156 1206 1 20 21 223 Oct. 13, 1999 258 HJPCP42 PTA-843 Uni-ZAP XR 746 1201 1 1201 134 1684 1 20 21 223 Oct. 13, 1999 258 HJPCP42 PTA-843 Uni-ZAP XR 747 628 229 628 468 1685 1 8 Oct. 13, 1999 258 HJPCP42 PTA-843 Uni-ZAP XR 748 425 237 348 1 1686 1 1 2 83 Oct. 13, 1999 259 HKAAE44 209368 Oct. 16, 1997 pCMVSport 2.0 269 1494 1 1494 113 113 1207 1 39 40 136 260 HKAAH36 209563 Dec. 18, 1997 pCMVSport 2.0 270 1216 1 1216 128 128 1208 1 29 30 293 260 HKAAH36 209563 Dec. 18, 1997 pCMVSport 2.0 749 1016 1 1016 295 295 1687 1 29 30 143 260 HKAAH36 209563 Dec. 18, 1997 pCMVSport 2.0 750 1490 1 1490 182 182 1688 1 29 30 293 260 HKAAH36 209563 Dec. 18, 1997 pCMVSport 2.0 751 1441 8 1392 184 184 1689 1 29 30 85 260 HKAAH36 209563 Dec. 18, 1997 pCMVSport 2.0 752 1516 1 1516 254 254 1690 1 29 30 293 260 HKAAH36 209563 Dec. 18, 1997 pCMVSport 2.0 753 1381 196 1381 129 129 1691 1 29 30 293 260 HKAAH36 209563 Dec. 18, 1997 pCMVSport 2.0 754 1439 1 1439 189 189 1692 1 29 30 61 261 HKAAK02 209551 Dec. 12, 1997 pCMVSport 2.0 271 859 1 859 97 97 1209 1 34 35 196 262 HKABI84 209603 Jan. 29, 1998 pCMVSport 2.0 272 1238 45 1238 274 274 1210 1 16 17 47 263 HKABZ65 209683 Mar. 20, 1998 pCMVSport 2.0 273 1189 1 1189 77 77 1211 1 17 18 243 263 HKABZ65 209683 Mar. 20, 1998 pCMVSport 2.0 755 1191 1 1191 69 69 1693 1 17 18 243 264 HKACB56 209346 Oct. 09, 1997 pCMVSport 2.0 274 496 1 496 27 27 1212 1 23 24 80 265 HKACD58 209346 Oct. 09, 1997 pCMVSport 2.0 275 3153 1 3153 38 38 1213 1 25 26 301 265 HKACD58 209346 Oct. 09, 1997 pCMVSport 2.0 756 1626 1 1626 35 35 1694 1 25 26 154 266 HKACH44 209300 Sep. 25, 1997 pCMVSport 2.0 276 686 1 686 375 375 1214 1 25 26 44 267 HKACM93 PTA-849 pCMVSport 2.0 277 2352 1 2352 218 218 1215 1 30 31 692 Oct. 13, 1999 267 HKACM93 PTA-849 pCMVSport 2.0 757 549 1 549 189 189 1695 1 30 31 120 Oct. 13, 1999 267 HKACM93 PTA-849 pCMVSport 2.0 758 1120 1 1120 314 314 1696 1 30 31 269 Oct. 13, 1999 267 HKACM93 PTA-849 pCMVSport 2.0 759 1893 739 1893 202 1697 1 13 14 17 Oct. 13, 1999 267 HKACM93 PTA-849 pCMVSport 2.0 760 1187 1 1187 638 1698 1 4 5 45 Oct. 13, 1999 268 HKAEL80 209423 Oct. 30, 1997 pCMVSport 2.0 278 1105 1 1105 398 398 1216 1 17 18 79 269 HKAEV06 209627 Feb. 12, 1998 pCMVSport 2.0 279 2496 1 2496 501 501 1217 1 30 31 438 269 HKAEV06 209627 Feb. 12, 1998 pCMVSport 2.0 761 2351 1 2351 197 197 1699 1 29 30 57 270 HKAFK41 209300 Sep. 25, 1997 pCMVSport 2.0 280 549 1 549 243 243 1218 1 30 31 43 271 HKAFT66 PTA-849 pCMVSport 2.0 281 1001 270 1001 508 508 1219 1 41 42 107 Oct. 13, 1999 271 HKAFT66 PTA-849 pCMVSport 2.0 762 1001 270 1001 508 508 1700 1 41 42 107 Oct. 13, 1999 271 HKAFT66 PTA-849 pCMVSport 2.0 763 669 1 669 234 234 1701 1 37 Oct. 13, 1999 272 HKDBF34 209511 Dec. 03, 1997 pCMVSport 1 282 1432 60 1418 69 69 1220 1 14 15 222 272 HKDBF34 209511 Dec. 03, 1997 pCMVSport 1 764 1356 1 1356 18 18 1702 1 19 20 104 273 HKGAT94 209126 Jun. 19, 1997 pSport1 283 1048 1 1048 449 449 1221 1 31 32 99 273 HKGAT94 209126 Jun. 19, 1997 pSport1 765 1063 1 1063 470 1702 1 20 21 94 274 HKGCO27 209853 May 07, 1998 pSport1 284 1021 1 1021 313 313 1222 1 26 27 93 274 HKGCO27 209853 May 07, 1998 pSport1 766 1311 1 1311 57 57 1704 1 26 27 47 275 HKISB57 209603 Jan. 29, 1998 pBLUESCRIPT ™ 285 1492 1 1439 130 130 1223 1 19 20 95 276 HKMLK53 209511 Dec. 03, 1997 pBLUESCRIPT ™ 286 1543 1 1543 20 20 1224 1 25 26 69 277 HKMLM11 209236 Sep. 04, 1997 pBLUESCRIPT ™ 287 954 1 954 82 82 1225 1 20 21 130 278 HKMLP68 PTA-845 pBLUESCRIPT ™ 288 2784 1 2784 130 130 1226 1 24 25 80 Oct. 13, 1999 278 HKMLP68 PTA-845 pBLUESCRIPT ™ 767 718 1 718 153 153 1705 1 24 25 80 Oct. 13, 1999 278 HKMLP68 PTA-845 pBLUESCRIPT ™ 768 614 1 614 471 1706 1 1 2 47 Oct. 13, 1999 279 HKMMD13 209568 Jan. 06, 1998 pBLUESCRIPT ™ 289 943 1 943 342 342 1227 1 21 22 49 280 HKMND01 203069 Jul. 27, 1998 pBLUESCRIPT ™ 290 887 1 887 23 23 1228 1 26 27 50 281 HL2AC08 209580 Jan. 14, 1998 Uni-ZAP XR 291 1478 1 1478 64 64 1229 1 23 24 280 282 HL2AG57 209746 Apr. 07, 1998 Uni-ZAP XR 292 1780 349 1780 560 560 1230 1 31 32 80 283 HLCND09 PTA-2076 Uni-ZAP XR 293 1984 1 1984 146 146 1231 1 38 39 110 Jun. 09, 2000 283 HLCND09 PTA-2076 Uni-ZAP XR 769 465 1 465 38 38 1707 1 38 39 142 Jun. 09, 2000 284 HLDBE54 209563 Dec. 18, 1997 pCMVSport 3.0 294 1222 1 1222 155 155 1232 1 38 39 318 284 HLDBE54 209563 Dec. 18, 1997 pCMVSport 3.0 770 1194 1 1194 130 130 1708 1 26 27 89 284 HLDBE54 209563 Dec. 18, 1997 pCMVSport 3.0 771 2334 1874 2334 133 133 1709 1 33 34 486 285 HLDBX13 203331 Oct. 08, 1998 pCMVSport 3.0 295 1815 1 1815 303 303 1233 1 39 40 55 286 HLDNA86 209277 Sep. 18, 1997 pCMVSport 3.0 296 1346 1 1346 238 238 1234 1 34 35 163 286 HLDNA86 209277 Sep. 18, 1997 pCMVSport 3.0 772 720 1 717 45 45 1710 1 31 32 92 287 HLDON23 209628 Feb. 12, 1998 pCMVSport 3.0 297 1262 208 1256 368 368 1235 1 20 21 113 288 HLDOW79 PTA-1544 pCMVSport 3.0 298 989 1 989 43 43 1236 1 21 22 275 Mar. 21, 2000 289 HLDQC46 PTA-1544 pCMVSport 3.0 299 632 1 632 163 163 1237 1 34 35 87 Mar. 21, 2000 290 HLDQR62 203027 Jun. 26, 1998 pCMVSport 3.0 300 2572 427 2572 520 520 1238 1 18 19 161 291 HLDQU79 203071 Jul. 27, 1998 pCMVSport 3.0 301 1488 1 1488 99 99 1239 1 23 24 348 292 HLDRM43 209628 Feb. 12, 1998 pCMVSport 3.0 302 609 1 609 24 24 1240 1 20 21 151 292 HLDRM43 209628 Feb. 12, 1998 pCMVSport 3.0 773 759 1 759 164 164 1711 1 20 21 151 293 HLDRP33 209641 Feb. 25, 1998 pCMVSport 3.0 303 612 1 612 215 215 1241 1 26 27 41 294 HLHFP03 209126 Jun. 19, 1997 Uni-ZAP XR 304 613 1 613 224 224 1242 1 19 20 116 295 HLHFR58 PTA-841 Uni-ZAP XR 305 1015 1 1015 206 1243 1 17 18 21 Oct. 13, 1999 295 HLHFR58 PTA-841 Uni-ZAP XR 774 733 1 733 205 1712 1 16 17 21 Oct. 13, 1999 295 HLHFR58 PTA-841 Uni-ZAP XR 775 741 1 741 288 1713 1 1 2 67 Oct. 13, 1999 295 HLHFR58 PTA-841 Uni-ZAP XR 776 951 12 675 254 1714 1 1 2 91 Oct. 13, 1999 296 HLIBD68 203071 Jul. 27, 1998 pCMVSport 1 306 1022 1 1022 186 186 1244 1 35 36 50 297 HLICQ90 203517 Dec. 10, 1998 pCMVSport 1 307 1766 1 1766 249 249 1245 1 29 30 206 298 HLMBO76 209603 Jan. 29, 1998 Lambda ZAP II 308 815 1 795 43 43 1246 1 43 44 107 299 HLQBE09 209243 Sep. 12, 1997 Lambda ZAP II 309 633 1 633 17 17 1247 1 19 20 181 300 HLQDR48 209603 Jan. 29, 1998 Lambda ZAP II 310 989 1 989 10 10 1248 1 21 22 190 300 HLQDR48 209603 Jan. 29, 1998 Lambda ZAP II 777 990 1 990 3 3 1715 1 21 22 190 301 HLTAU74 PTA-163 Uni-ZAP XR 311 1524 1 1524 76 76 1249 1 21 22 62 Jun. 01, 1999 302 HLTDV50 209243 Sep. 12, 1997 Uni-ZAP XR 312 770 1 770 74 74 1250 1 17 18 28 303 HLTEI25 97979 Mar. 27, 1997 Uni-ZAP XR 313 843 1 843 155 155 1251 1 19 20 42 304 HLTEJ06 209346 Oct. 09, 1997 Uni-ZAP XR 314 617 69 617 197 197 1252 1 22 23 55 305 HLTFA64 209628 Feb. 12, 1998 Uni-ZAP XR 315 1130 1 1130 268 268 1253 1 42 43 43 306 HLTHG37 209965 Jun. 11, 1998 Uni-ZAP XR 316 3740 1908 3740 50 50 1254 1 1 2 319 306 HLTHG37 209965 Jun. 11, 1998 Uni-ZAP XR 778 1932 98 1932 313 313 1716 1 35 36 42 307 HLWAA17 209626 Feb. 12, 1998 pCMVSport 3.0 317 997 246 997 436 436 1255 1 15 16 187 308 HLWAA88 209551 Dec. 12, 1997 pCMVSport 3.0 318 1770 1 1770 35 35 1256 1 22 23 113 308 HLWAA88 209551 Dec. 12, 1997 pCMVSport 3.0 779 1636 1 1636 51 51 1717 1 22 23 488 309 HLWAD77 209651 Mar. 04, 1998 pCMVSport 3.0 319 1167 304 1167 326 326 1257 1 24 25 140 310 HLWAE11 203071 Jul. 27, 1998 pCMVSport 3.0 320 1618 1 1618 28 28 1258 1 46 47 278 311 HLWAO22 209511 Dec. 03, 1997 pCMVSport 3.0 321 1338 1 1311 212 212 1259 1 21 22 354 312 HLWAY54 209651 Mar. 04, 1998 pCMVSport 3.0 322 1892 1 1892 38 38 1260 1 25 26 338 313 HLWBH18 PTA-849 pCMVSport 3.0 323 813 1 813 107 107 1261 1 18 19 60 Oct. 13, 1999 313 HLWBH18 PTA-849 pCMVSport 3.0 780 645 1 645 67 67 1718 1 18 19 60 Oct. 13, 1999 314 HLWBI63 209407 Oct. 23, 1997 pCMVSport 3.0 324 1038 1 1038 149 149 1262 1 30 31 63 315 HLWBK05 203331 Oct. 08, 1998 pCMVSport 3.0 325 2383 157 2383 280 280 1263 1 34 35 298 316 HLWBY76 203517 Dec. 10, 1998 pCMVSport 3.0 326 2081 1 2081 432 432 1264 1 27 28 232 317 HLWCF05 209126 Jun. 19, 1997 pCMVSport 3.0 327 646 1 646 155 155 1265 1 36 37 58 318 HLYAC95 203071 Jul. 27, 1998 pSport1 328 312 1 312 92 92 1266 1 16 17 46 319 HLYAF80 209126 Jun. 19, 1997 pSport1 329 826 1 826 222 222 1267 1 24 25 47 320 HLYAN59 209346 Oct. 09, 1997 pSport1 330 770 1 770 383 383 1268 1 40 41 77 320 HLYAN59 209346 Oct. 09, 1997 pSport1 781 729 1 729 254 254 1719 1 39 40 54 321 HLYAP91 209346 Oct. 09, 1997 pSport1 331 1276 1 1276 280 280 1269 1 29 30 83 322 HLYAZ61 209022 May 08, 1997 pSport1 332 1237 1 1237 190 190 1270 1 18 19 222 322 HLYAZ61 209022 May 08, 1997 pSport1 782 997 74 997 205 205 1720 1 18 19 215 323 HLYBD32 209407 Oct. 23, 1997 pSport1 333 1045 35 1045 98 98 1271 1 23 24 70 324 HLYES38 209853 May 07, 1998 pSport1 334 1223 1 1223 69 69 1272 1 22 23 73 325 HMADS41 209563 Dec. 18, 1997 Uni-ZAP XR 335 1267 1 1267 267 267 1273 1 21 22 88 326 HMADU73 209139 Jul. 03, 1997 Uni-ZAP XR 336 3194 1 3194 491 491 1274 1 16 17 713 326 HMADU73 209139 Jul. 03, 1997 Uni-ZAP XR 783 437 1 437 115 115 1721 1 15 16 77 327 HMAMI15 PTA-2075 Uni-ZAP XR 337 1258 1 1258 4 4 1275 1 26 27 340 Jun. 09, 2000 327 HMAMI15 PTA-2075 Uni-ZAP XR 784 1084 1 1084 3 3 1722 1 26 27 306 Jun. 09, 2000 328 HMDAE65 209243 Sep. 12, 1997 Uni-ZAP XR 338 698 1 698 179 179 1276 1 17 18 77 329 HMDAM24 209226 Aug. 28, 1997 Uni-ZAP XR 339 996 1 996 109 109 1277 1 20 330 HMDAQ29 209563 Dec. 18, 1997 Uni-ZAP XR 340 974 1 974 180 180 1278 1 43 44 82 331 HMEAI48 203069 Jul. 27, 1998 Lambda ZAP II 341 413 1 413 36 36 1279 1 29 30 88 331 HMEAI48 203069 Jul. 27, 1998 Lambda ZAP II 785 1168 1 1168 95 95 1723 1 29 30 40 332 HMECK83 209853 May 07, 1998 Lambda ZAP II 342 1010 1 1010 50 50 1280 1 28 29 54 333 HMEET96 209407 Oct. 23, 1997 Lambda ZAP II 343 1337 73 1200 121 121 1281 1 30 31 266 334 HMIAL37 209563 Dec. 18, 1997 Uni-ZAP XR 344 1420 1 1420 49 49 1282 1 13 14 97 335 HMIAP86 209878 May 18, 1998 Uni-ZAP XR 345 1674 13 1674 182 182 1283 1 19 20 334 336 HMKCG09 209346 Oct. 09, 1997 pSport1 346 921 60 921 221 221 1284 1 28 29 49 337 HMMAH60 209368 Oct. 16, 1997 pSport1 347 822 1 822 142 142 1285 1 15 16 50 338 HMQDF12 209407 Oct. 23, 1997 Uni-ZAP XR 348 706 1 627 63 63 1286 1 27 28 142 339 HMSBX80 209563 Dec. 18, 1997 Uni-ZAP XR 349 1726 1 1726 169 169 1287 1 19 20 57 340 HMSFS21 209324 Oct. 02, 1997 Uni-ZAP XR 350 1283 1 1283 28 28 1288 1 17 18 37 341 HMSGB14 209423 Oct. 30, 1997 Uni-ZAP XR 351 1552 1 1552 138 138 1289 1 18 19 77 342 HMSGT42 97958 Mar. 13, 1997 Uni-ZAP XR 352 1563 33 1077 40 40 1290 1 32 33 92 209072 May 22, 1997 343 HMSHM14 209126 Jun. 19, 1997 Uni-ZAP XR 353 756 1 756 103 103 2191 1 29 30 45 344 HMSHS36 PTA-2070 Uni-ZAP XR 354 1402 1 1402 134 134 1292 1 23 24 103 Jun. 09, 2000 344 HMSHS36 PTA-2070 Uni-ZAP XR 786 616 30 616 162 162 1724 1 23 24 103 Jun. 09, 2000 345 HMSJM65 209641 Feb. 25, 1998 Uni-ZAP XR 355 2270 1 2231 111 111 1293 1 27 28 77 346 HMSJU68 209076 May 22, 1997 Uni-ZAP XR 356 1123 4 1123 272 272 1294 1 31 32 49 347 HMSKC04 203105 Aug. 13, 1998 Uni-ZAP XR 357 1417 1 1417 133 133 1295 1 22 23 73 348 HMTBI36 PTA-322 pCMVSport 3.0 358 3388 1 3388 256 256 1296 1 18 19 957 Jul. 09, 1999 348 HMTBI36 PTA-322 pCMVSport 3.0 787 3546 1 3363 255 255 1725 1 18 19 957 Jul. 09, 1999 349 HMUAP70 209878 May 18, 1998 pCMVSport 3.0 359 1965 531 1914 183 183 1297 1 16 17 221 349 HMUAP70 209878 May 18, 1998 pCMVSport 3.0 788 1842 407 1783 413 413 1726 1 25 26 103 349 HMUAP70 209878 May 18, 1998 pCMVSport 3.0 789 1963 530 1914 251 251 1727 1 28 29 198 349 HMUAP70 209878 May 18, 1998 pCMVSport 3.0 790 1487 1 1487 62 62 1728 1 16 17 106 349 HMUAP70 209878 May 18, 1998 pCMVSport 3.0 791 1653 1 1653 60 60 1729 1 15 16 68 349 HMUAP70 209878 May 18, 1998 pCMVSport 3.0 792 1830 407 1830 60 60 1730 1 23 350 HMVBN46 209603 Jan. 29, 1998 pSport1 360 1382 1 1382 10 10 1298 1 19 20 48 351 HMWEB02 209628 Feb. 12, 1998 Uni-ZAP XR 361 1755 1 1755 106 106 1299 1 23 24 91 352 HMWFO02 209324 Oct. 02, 1997 Uni-ZAP XR 362 547 1 547 7 7 1300 1 37 38 68 352 HMWFO02 209324 Oct. 02, 1997 Uni-ZAP XR 793 708 1 708 20 20 1731 1 38 39 60 353 HMWGY65 203105 Aug. 13, 1998 Uni-ZAP XR 363 1974 1 1974 42 42 1301 1 21 22 490 353 HMWGY65 203105 Aug. 13, 1998 Uni-ZAP XR 794 2027 1 1976 42 42 1732 1 21 22 188 354 HNEAC05 209236 Sep. 04, 1997 Uni-ZAP XR 364 890 1 890 101 101 1302 1 24 25 105 355 HNEEB45 PTA-845 Uni-ZAP XR 365 1043 1 1043 139 139 1303 1 25 26 57 Oct. 13, 1999 355 HNEEB45 PTA-845 Uni-ZAP XR 795 699 160 699 226 226 1733 1 25 26 57 Oct. 13, 1999 356 HNFFC43 203027 Jun. 26, 1998 Uni-ZAP XR 366 2103 209 2058 488 488 1304 1 12 13 68 357 HNFIU96 209126 Jun. 19, 1997 pBLUESCRIPT ™ 367 456 1 456 170 170 1305 1 32 33 79 358 HNFJF07 209463 Nov. 14, 1997 Uni-ZAP XR 368 616 1 616 86 86 1306 1 21 22 66 359 HNFJH45 97976 Apr. 04, 1997 Uni-ZAP XR 369 575 1 575 275 275 1307 1 30 31 67 360 HNGAK47 209368 Oct. 16, 1997 Uni-ZAP XR 370 1144 1 1144 89 89 1308 1 23 24 40 361 HNGAP93 209243 Sep. 12, 1997 Uni-ZAP XR 371 703 1 703 50 50 1309 1 19 20 33 362 HNGBC07 PTA-844 Uni-ZAP XR 372 1649 1 1647 81 81 1310 1 18 19 249 Oct. 13, 1999 362 HNGBC07 PTA-844 Uni-ZAP XR 796 1649 1 1647 122 122 1734 1 24 25 44 Oct. 13, 1999 362 HNGBC07 PTA-844 Uni-ZAP XR 797 1570 1 1570 55 55 1735 1 24 25 44 Oct. 13, 1999 363 HNGBT31 97976 Apr. 04, 1997 Uni-ZAP XR 373 639 1 639 224 224 1311 1 28 29 104 364 HNGDG40 209299 Sep. 25, 1997 Uni-ZAP XR 374 520 1 520 13 13 1312 1 36 37 127 365 HNGDJ72 209299 Sep. 25, 1997 Uni-ZAP XR 375 524 1 524 185 185 1313 1 19 20 113 366 HNGDU40 209563 Dec. 18, 1997 Uni-ZAP XR 376 1035 1 1035 333 333 1314 1 17 18 51 367 HNGEO29 209299 Sep. 25, 1997 Uni-ZAP XR 377 491 1 491 98 98 1315 1 32 33 44 368 HNGEP09 209197 Aug. 08, 1997 Uni-ZAP XR 378 1042 1 1042 72 72 1316 1 15 16 82 369 HNGHR74 209346 Oct. 09, 1997 Uni-ZAP XR 379 1095 1 1095 53 53 1317 1 18 19 41 370 HNGIH43 97976 Apr. 04, 1997 Uni-ZAP XR 380 427 1 427 178 178 1318 1 31 32 40 371 HNGIJ31 209236 Sep. 04, 1997 Uni-ZAP XR 381 796 1 796 135 135 1319 1 16 17 36 372 HNGIQ46 209243 Sep. 12, 1997 Uni-ZAP XR 382 527 1 527 221 221 1320 1 21 22 70 373 HNGJE50 209368 Oct. 16, 1997 Uni-ZAP XR 383 1037 1 1037 77 77 1321 1 36 37 46 374 HNGJO57 209463 Nov. 14, 1997 Uni-ZAP XR 384 828 1 828 87 87 1322 1 18 19 52 375 HNGJP69 209603 Jan. 29, 1998 Uni-ZAP XR 385 985 1 985 321 321 1323 1 14 15 74 376 HNGJT54 209215 Aug. 21, 1997 Uni-ZAP XR 386 1110 1 1110 172 172 1324 1 19 20 34 377 HNGKN89 203648 Feb. 09, 1999 Uni-ZAP XR 387 925 1 925 436 436 1325 1 24 25 53 378 HNGOM56 203648 Feb. 09, 1999 Uni-ZAP XR 388 956 1 956 391 391 1326 1 22 23 55 379 HNGOU56 203858 Mar. 18, 1999 Uni-ZAP XR 389 742 1 742 317 317 1327 1 23 24 59 380 HNGOW62 PTA-622 Uni-ZAP XR 390 1298 1 1298 167 167 1328 1 19 20 54 Sep. 02, 1999 381 HNHAH01 209180 Jul. 24, 1997 Uni-ZAP XR 391 905 1 905 328 328 1329 1 41 42 54 382 HNHCX60 209243 Sep. 12, 1997 Uni-ZAP XR 392 762 1 762 158 158 1330 1 20 21 21 383 HNHCY64 209243 Sep. 12, 1997 Uni-ZAP XR 393 725 1 725 258 258 1331 1 32 33 44 384 HNHCY94 209243 Sep. 12, 1997 Uni-ZAP XR 394 606 1 606 78 78 1332 1 25 26 48 385 HNHDW38 209299 Sep. 25, 1997 Uni-ZAP XR 395 793 1 793 231 231 1333 1 22 23 46 386 HNHDW42 97976 Apr. 04, 1997 Uni-ZAP XR 396 426 1 426 168 168 1334 1 26 27 71 387 HNHED17 209346 Oct. 09, 1997 Uni-ZAP XR 397 843 1 843 274 274 1335 1 19 20 51 387 HNHED17 209346 Oct. 09, 1997 Uni-ZAP XR 798 692 1 692 282 282 1736 1 19 20 48 388 HNHEI42 PTA-844 Uni-ZAP XR 398 2642 1 2642 52 52 1336 1 22 23 36 Oct. 13, 1999 388 HNHEI42 PTA-844 Uni-ZAP XR 799 1654 1 1654 28 28 1737 1 22 23 36 Oct. 13, 1999 388 HNHEI42 PTA-844 Uni-ZAP XR 800 447 1 447 166 1738 1 6 7 28 Oct. 13, 1999 388 HNHEI42 PTA-844 Uni-ZAP XR 801 641 1 641 331 1739 1 3 4 34 Oct. 13, 1999 389 HNHFO29 209138 Jul. 03, 1997 Uni-ZAP XR 399 699 1 699 160 160 1337 1 21 22 180 390 HNHFR04 209683 Mar. 20, 1998 Uni-ZAP XR 400 1681 1 1681 71 71 1338 1 21 22 78 391 HNHFU32 209407 Oct. 23, 1997 Uni-ZAP XR 401 607 1 607 175 175 1339 1 30 31 52 392 HNHOD46 PTA-1543 Uni-ZAP XR 402 1355 1 1355 12 12 1340 1 20 21 80 Mar. 21, 2000 393 HNHOG73 203570 Jan. 11, 1999 Uni-ZAP XR 403 802 1 802 342 342 1341 1 19 20 51 394 HNHPD10 203570 Jan. 11, 1999 Uni-ZAP XR 404 940 1 940 291 291 1342 1 33 34 40 395 HNTBI57 209423 Oct. 30, 1997 pCMVSport 3.0 405 1365 134 1365 210 210 1343 1 26 27 58 396 HNTCE26 PTA-1544 pCMVSport 3.0 406 2163 830 2163 111 111 1344 1 30 31 402 Mar. 21, 2000 396 HNTCE26 PTA-1544 pCMVSport 3.0 801 1763 1 1763 57 57 1740 1 28 29 121 Mar. 21, 2000 397 HNTNC20 209782 Apr. 20, 1998 pSport1 407 1979 1 1979 270 270 1345 1 19 20 218 398 HNTNI01 209782 Apr. 20, 1998 pSport1 408 2087 1 2087 307 307 1346 1 33 34 76 398 HNTNI01 209782 Apr. 20, 1998 pSport1 803 1274 1 1114 306 306 1741 1 33 34 49 399 HNTSY18 PTA-855 pSport1 409 1811 265 1783 257 257 1347 1 31 32 89 Oct. 18, 1999 399 HNTSY18 PTA-855 pSport1 804 847 742 819 420 1742 1 1 2 79 Oct. 18, 1999 400 HOAAC90 209236 Sep. 04, 1997 Uni-ZAP XR 410 642 1 642 33 33 1348 1 15 16 104 400 HOAAC90 209236 Sep. 04, 1997 Uni-ZAP XR 805 652 1 652 38 38 1743 1 15 16 104 401 HOACB38 209243 Sep. 12, 1997 Uni-ZAP XR 411 606 1 606 63 63 1349 1 21 22 40 402 HOCNF19 203570 Jan. 11, 1999 pSport1 412 1118 1 1118 166 166 1350 1 20 21 87 403 HODDF13 203069 Jul. 27, 1998 Uni-ZAP XR 413 830 1 830 46 46 1351 1 23 24 41 404 HODDN65 209244 Sep. 12, 1997 Uni-ZAP XR 414 755 1 755 251 251 1352 1 14 15 20 405 HODDN92 209012 Apr. 28, 1997 Uni-ZAP XR 415 1939 294 1939 434 1553 1 26 27 35 209089 Jun. 05, 1997 406 HODDO08 203364 Oct. 19, 1998 Uni-ZAP XR 416 1776 138 1284 725 725 1354 1 33 34 106 407 HODDW40 209463 Nov. 14, 1997 Uni-ZAP XR 417 682 1 682 139 139 1355 1 19 20 40 408 HODEJ32 203570 Jan. 11, 1999 Uni-ZAP XR 418 739 1 739 358 358 1356 1 21 22 43 409 HODFN71 203570 Jan. 11, 1999 Uni-ZAP XR 419 1126 1 1126 1 1357 1 1 2 159 409 HODFN71 203570 Jan. 11, 1999 Uni-ZAP XR 806 1124 1 1124 27 27 1744 1 18 19 148 410 HODGE68 203570 Jan. 11, 1999 Uni-ZAP XR 420 851 1 851 87 87 1358 1 26 27 59 411 HOEBK34 209224 Aug. 28, 1997 Uni-ZAP XR 421 747 75 747 149 149 1359 1 20 21 165 411 HOEBK34 209224 Aug. 28, 1997 Uni-ZAP XR 807 660 1 660 68 68 1745 1 26 27 88 412 HOEBZ89 203517 Dec. 10, 1998 Uni-ZAP XR 422 2520 1 2520 19 19 1360 1 21 22 333 413 HOEDB32 209628 Feb. 12, 1998 Uni-ZAP XR 423 1462 73 1462 104 104 1361 1 21 22 226 414 HOEDE28 PTA-844 Uni-ZAP XR 424 1635 1 1635 248 248 1362 1 21 22 117 Oct. 13, 1999 414 HOEDE28 PTA-844 Uni-ZAP XR 808 1424 806 1424 387 1746 1 11 12 20 Oct. 13, 1999 415 HOEDH84 209965 Jun. 11, 1998 Uni-ZAP XR 425 2079 1 2079 256 256 1363 1 20 21 404 416 HOEFV61 203517 Dec. 10, 1998 Uni-ZAP XR 426 2657 1 2657 64 64 1364 1 13 14 180 417 HOFMQ33 PTA-848 pCMVSport 2.0 427 2410 1 2410 49 49 1365 1 24 25 484 Oct. 13, 1999 417 HOFMQ33 PTA-848 pCMVSport 2.0 809 2409 1 2409 48 48 1747 1 24 25 484 Oct. 13, 1999 417 HOFMQ33 PTA-848 pCMVSport 2.0 810 876 1 876 78 78 1748 1 24 25 266 Oct. 13, 1999 417 HOFMQ33 PTA-848 pCMVSport 2.0 811 1586 1 1586 724 1749 1 5 Oct. 13, 1999 417 HOFMQ33 PTA-848 pCMVSport 2.0 812 1011 873 1011 123 1750 1 1 2 84 Oct. 13, 1999 418 HOFMT75 PTA-848 pCMVSport 2.0 428 2131 6 2131 83 83 1366 1 20 21 410 Oct. 13, 1999 418 HOFMT75 PTA-848 pCMVSport 2.0 813 427 1 427 83 83 1751 1 20 21 115 Oct. 13, 1999 418 HOFMT75 PTA-848 pCMVSport 2.0 814 1500 1 1500 1225 1752 1 9 10 92 Oct. 13, 1999 418 HOFMT75 PTA-848 pCMVSport 2.0 815 1234 337 1234 129 129 1753 1 20 21 368 Oct. 13, 1999 419 HOFNC14 PTA-623 pCMVSport 2.0 429 2794 1 2794 79 79 1367 1 13 14 73 Sep. 02, 1999 419 HOFNC14 PTA-623 pCMVSport 2.0 816 3095 1 3095 155 155 1754 1 13 14 72 Sep. 02, 1999 420 HOFND85 PTA-1544 pCMVSport 2.0 430 2048 1 2048 167 167 1368 1 22 23 627 Mar. 21, 2000 421 HOFNY91 PTA-1544 pCMVSport 2.0 431 2406 1 2406 64 64 1369 1 14 15 82 Mar. 21, 2000 422 HOFOC33 PTA-848 pCMVSport 2.0 432 1669 1 1669 76 76 1370 1 21 22 363 Oct. 13, 1999 422 HOFOC33 PTA-848 pCMVSport 2.0 817 518 1 518 81 81 1755 1 21 22 112 Oct. 13, 1999 422 HOFOC33 PTA-848 pCMVSport 2.0 818 518 1 518 81 81 1756 1 17 18 112 Oct. 13, 1999 422 HOFOC33 PTA-848 pCMVSport 2.0 819 1670 1 1670 76 76 1757 1 21 22 139 Oct. 13, 1999 422 HOFOC33 PTA-848 pCMVSport 2.0 820 606 1 606 23 1758 1 7 Oct. 13, 1999 422 HOFOC33 PTA-848 pCMVSport 2.0 821 841 1 841 158 1759 1 6 7 14 Oct. 13, 1999 422 HOFOC33 PTA-848 pCMVSport 2.0 822 868 1 847 3 1760 1 1 2 288 Oct. 13, 1999 423 HOFOC73 PTA-848 pCMVSport 2.0 433 1491 1 1491 18 18 1371 1 18 19 129 Oct. 13, 1999 423 HOFOC73 PTA-848 pCMVSport 2.0 823 1395 1 1395 23 23 1761 1 18 19 67 Oct. 13, 1999 423 HOFOC73 PTA-848 pCMVSport 2.0 824 270 1 270 127 1762 1 4 5 14 Oct. 13, 1999 423 HOFOC73 PTA-848 pCMVSport 2.0 825 2324 662 2324 142 142 1763 1 6 Oct. 13, 1999 424 HOGAW62 209463 Nov. 14, 1997 pCMVSport 2.0 434 571 1 571 259 259 1372 1 25 26 55 425 HOGCK20 209853 May 07, 1998 pCMVSport 2.0 435 2087 1 2087 57 57 1373 1 23 24 522 425 HOGCK20 209853 May 07, 1998 pCMVSport 2.0 826 2075 1 2054 53 1764 1 22 23 554 426 HOGCK63 PTA-848 pCMVSport 2.0 436 1409 310 1409 514 514 1374 1 29 30 246 Oct. 13, 1999 426 HOGCK63 PTA-848 pCMVSport 2.0 827 1697 144 1697 1455 1765 1 5 Oct. 13, 1999 427 HOGCS52 PTA-848 pCMVSport 2.0 437 2571 1 2571 25 25 1375 1 22 23 453 Oct. 13, 1999 427 HOGCS52 PTA-848 pCMVSport 2.0 828 2645 1 2586 30 30 1766 1 22 23 453 Oct. 13, 1999 427 HOGCS52 PTA-848 pCMVSport 2.0 829 1098 457 638 2 1767 1 1 2 96 Oct. 13, 1999 428 HOHBB49 203517 Dec. 10, 1998 pCMVSport 2.0 438 3080 1 3080 148 148 1376 1 19 20 48 429 HOHBC68 209568 Jan. 06, 1998 pCMVSport 2.0 439 1837 1 1837 348 348 1377 1 30 31 128 430 HOHBY12 209603 Jan. 29, 1998 pCMVSport 2.0 440 1188 1 1188 232 232 1378 1 25 26 199 431 HOHBY44 PTA-867 pCMVSport 2.0 441 3369 1 3369 170 170 1379 1 24 25 184 Oct. 26, 1999 431 HOHBY44 PTA-867 pCMVSport 2.0 830 1063 533 1063 2 1768 1 1 2 77 Oct. 26, 1999 431 HOHBY44 PTA-867 pCMVSport 2.0 831 1178 1 1178 54 1769 1 1 2 84 Oct. 26, 1999 432 HOHCC74 209346 Oct. 09, 1997 pCMVSport 2.0 442 558 1 558 327 327 1380 1 20 21 48 433 HOHCH55 203331 Oct. 08, 1998 pCMVSport 2.0 443 2499 1 2499 221 221 1381 1 23 24 494 433 HOHCH55 203331 Oct. 08, 1998 pCMVSport 2.0 832 2522 1 2522 230 230 1770 1 23 24 469 434 HONAH29 209138 Jul. 03, 1997 pBLUESCRIPT ™ 444 1623 1 1623 136 136 1382 1 25 26 211 SK− 434 HONAH29 209138 Jul. 03, 1997 pBLUESCRIPT ™ 833 1637 17 1632 144 144 1771 1 25 26 211 SK− 435 HOSDJ25 209423 Oct. 30, 1997 Uni-ZAP XR 445 2214 985 2214 1076 1076 1383 1 18 19 40 435 HOSDJ25 209423 Oct. 30, 1997 Uni-ZAP XR 834 1258 1 1258 146 146 1772 1 18 19 40 436 HOSEG51 209324 Oct. 02, 1997 Uni-ZAP XR 446 590 48 590 232 232 1384 1 31 32 102 437 HOSFD58 97957 Mar. 13, 1997 Uni-ZAP XR 447 2527 290 1747 56 56 1385 1 30 31 624 209073 May 22, 1997 437 HOSFD58 97957 Mar. 13, 1997 Uni-ZAP XR 835 2527 288 1747 477 477 1773 1 32 33 61 209073 May 22, 1997 438 HOUCQ17 209086 May 29, 1997 Uni-ZAP XR 448 4712 1 4693 508 508 1386 1 51 52 967 439 HOUDK26 209423 Oct. 30, 1997 Uni-ZAP XR 449 1051 1 1051 214 214 1387 1 30 31 174 440 HOVCA92 209299 Sep. 25, 1997 pSport1 450 707 1 488 181 181 1388 1 20 21 62 441 HPASA81 203181 Sep. 09, 1998 Uni-ZAP XR 451 1945 1 1945 19 19 1389 1 17 18 600 441 HPASA81 203181 Sep. 09, 1998 Uni-ZAP XR 836 1971 2 1971 14 14 1774 1 17 18 315 441 HPASA81 203181 Sep. 09, 1998 Uni-ZAP XR 837 2081 1 2081 124 124 1775 1 17 18 72 442 HPBCU51 97977 Apr. 04, 1997 pBLUESCRIPT ™ 452 599 1 599 86 86 1390 1 27 28 119 209082 May 29, 1997 SK− 443 HPDDC77 209012 Apr. 28, 1997 pBLUESCRIPT ™ 453 978 1 978 51 51 1391 1 29 30 131 209089 Jun. 05, 1997 SK− 443 HPDDC77 209012 Apr. 28, 1997 pBLUESCRIPT ™ 838 2361 455 1442 510 510 1776 1 29 30 131 209089 Jun. 05, 1997 SK− 444 HPDWP28 PTA-2076 pSport1 454 528 1 528 143 143 1392 1 29 30 49 Jun. 09, 2000 444 HPDWP28 PTA-2076 pSport1 839 510 1 500 133 133 1777 1 29 30 49 Jun. 09, 2000 445 HPEAD48 209244 Sep. 12, 1997 Uni-ZAP XR 455 625 1 625 203 203 1393 1 18 19 97 446 HPEBE79 209241 Sep. 12, 1997 Uni-ZAP XR 456 597 1 597 79 79 1394 1 11 12 15 447 HPFCL43 209299 Sep. 25, 1997 Uni-ZAP XR 457 665 1 665 21 21 1395 1 17 18 79 448 HPFDG48 209324 Oct. 02, 1997 Uni-ZAP XR 458 723 165 700 283 283 1396 1 18 19 47 449 HPIAQ68 203517 Dec. 10, 1998 Uni-ZAP XR 459 2466 1 2466 20 20 1397 1 22 23 62 450 HPIBO15 209563 Dec. 18, 1997 Uni-ZAP XR 460 1739 1 1739 128 128 1398 1 18 19 211 450 HPIBO15 209563 Dec. 18, 1997 Uni-ZAP XR 840 1739 1 1739 127 127 1778 1 18 19 173 451 HPICB53 PTA-846 Uni-ZAP XR 461 1139 1 1139 170 170 1399 1 23 24 51 Oct. 13, 1999 451 HPICB53 PTA-846 Uni-ZAP XR 841 438 1 438 163 163 1779 1 23 24 51 Oct. 13, 1999 452 HPJBK12 PTA-855 Uni-ZAP XR 462 2648 1 2648 126 126 1400 1 18 19 48 Oct. 18, 1999 452 HPJBK12 PTA-855 Uni-ZAP XR 842 538 1 538 119 119 1780 1 18 19 48 Oct. 18, 1999 452 HPJBK12 PTA-855 Uni-ZAP XR 843 1346 1 1346 969 1781 1 10 Oct. 18, 1999 452 HPJBK12 PTA-855 Uni-ZAP XR 844 912 1 912 509 509 1782 1 4 Oct. 18, 1999 453 HPJCL22 PTA-2071 Uni-ZAP XR 463 3107 1 3107 86 86 1401 1 35 36 80 Jun. 09, 2000 453 HPJCL22 PTA-2071 Uni-ZAP XR 845 995 58 995 136 136 1783 1 35 36 80 Jun. 09, 2000 453 HPJCL22 PTA-2071 Uni-ZAP XR 846 751 183 751 232 1784 1 1 2 145 Jun. 09, 2000 454 HPJCW04 209551 Dec. 12, 1997 Uni-ZAP XR 464 1466 1 1466 44 44 1402 1 19 20 57 455 HPJEX20 PTA-872 Uni-ZAP XR 465 566 1 566 23 23 1403 1 26 27 174 Oct. 26, 1999 455 HPJEX20 PTA-872 Uni-ZAP XR 847 1823 1 1823 31 31 1785 1 23 24 115 Oct. 26, 1999 455 HPJEX20 PTA-872 Uni-ZAP XR 848 1964 1 1964 170 170 1786 1 23 24 174 Oct. 26, 1999 455 HPJEX20 PTA-872 Uni-ZAP XR 849 769 1 769 84 84 1787 1 23 24 228 Oct. 26, 1999 455 HPJEX20 PTA-872 Uni-ZAP XR 850 818 1 818 565 1788 1 1 2 84 Oct. 26, 1999 456 HPMAI22 209683 Mar. 20, 1998 Uni-ZAP XR 466 1274 334 1274 483 483 1404 1 16 17 59 457 HPMFP40 209628 Feb. 12, 1998 Uni-ZAP XR 467 1217 1 1217 37 37 1405 1 24 25 44 458 HPMGJ45 203105 Aug. 13, 1998 Uni-ZAP XR 468 1656 1 1656 119 119 1406 1 25 26 48 459 HPQAC69 97979 Mar. 27, 1997 Lambda ZAP II 469 990 1 988 82 82 1407 1 19 20 37 460 HPRBC80 209852 May 07, 1998 Uni-ZAP XR 470 2543 1245 2543 94 94 1408 1 30 31 387 460 HPRBC80 209852 May 07, 1998 Uni-ZAP XR 851 2052 275 2032 404 404 1789 1 26 27 69 461 HPRBF19 203517 Dec. 10, 1998 Uni-ZAP XR 471 1461 1 1461 63 63 1409 1 31 32 190 462 HPTTG19 209628 Feb. 12, 1998 Uni-ZAP XR 472 559 1 559 215 215 1410 1 16 17 49 463 HPTVX32 209628 Feb. 12, 1998 pBLUESCRIPT ™ 473 803 215 803 318 318 1411 1 26 27 80 464 HPVAB94 209244 Sep. 12, 1997 Uni-ZAP XR 474 819 1 819 80 80 1412 1 25 26 44 465 HPWAY46 PTA-843 Uni-ZAP XR 475 1414 1 1414 468 468 1413 1 30 31 52 Oct. 13, 1999 465 HPWAY46 PTA-843 Uni-ZAP XR 852 891 1 891 474 474 1790 1 30 31 52 Oct. 13, 1999 465 HPWAY46 PTA-843 Uni-ZAP XR 853 501 120 501 178 1791 1 1 2 86 Oct. 13, 1999 466 HPWDJ42 209852 May 07, 1998 Uni-ZAP XR 476 1340 1 1340 149 149 1414 1 18 19 54 466 HPWDJ42 209852 May 07, 1998 Uni-ZAP XR 854 1340 1 1340 149 149 1792 1 21 22 54 466 HPWDJ42 209852 May 07, 1998 Uni-ZAP XR 855 813 1 813 161 161 1793 1 18 19 47 467 HPZAB47 209511 Dec. 03, 1997 pBLUESCRIPT ™ 477 1676 1 1676 34 34 1415 1 18 19 47 468 HRAAB15 209651 Mar. 04, 1998 pCMVSport 3.0 478 1747 1 1747 35 35 1416 1 14 15 159 469 HRABA80 209889 May 22, 1998 pCMVSport 3.0 479 1251 1 1251 144 144 1417 1 27 28 102 469 HRABA80 209889 May 22, 1998 pCMVSport 3.0 856 1237 1 1237 130 130 1794 1 27 28 102 470 HRACD15 209852 May 07, 1998 pCMVSport 3.0 480 1539 24 1539 252 252 1418 1 40 41 53 470 HRACD15 209852 May 07, 1998 pCMVSport 3.0 857 1681 24 1453 252 252 1795 1 40 41 53 471 HRACD80 209889 May 22, 1998 pCMVSport 3.0 481 1941 1 1941 196 196 1419 1 16 17 575 471 HRACD80 209889 May 22, 1998 pCMVSport 3.0 858 1934 1 1934 191 191 1796 1 16 17 575 471 HRACD80 209889 May 22, 1998 pCMVSport 3.0 859 1958 1 1958 191 191 1797 1 16 17 146 472 HRDDV47 209628 Feb. 12, 1998 Uni-ZAP XR 482 1510 1 1510 146 146 1420 1 30 31 276 473 HRDFD27 209423 Oct. 30, 1997 Uni-ZAP XR 483 805 1 805 82 82 1421 1 35 36 83 474 HROAJ03 209423 Oct. 30, 1997 Uni-ZAP XR 484 1182 1 1182 19 19 1422 1 20 21 192 475 HRTAE58 209241 Sep. 12, 1997 pBLUESCRIPT ™ 485 600 1 600 244 244 1423 1 18 19 58 SK− 476 HSATR82 209299 Sep. 25, 1997 Uni-ZAP XR 486 777 1 777 74 74 1424 1 15 16 41 477 HSAUK57 209148 Jul. 17, 1997 Uni-ZAP XR 487 1037 1 1037 322 322 1425 1 26 27 83 477 HSAUK57 209148 Jul. 17, 1997 Uni-ZAP XR 860 1070 1 1070 327 327 1798 1 26 27 48 478 HSAUL82 209148 Jul. 17, 1997 Uni-ZAP XR 488 727 1 727 140 140 1426 1 25 26 49 479 HSAVH65 209651 Mar. 04, 1998 Uni-ZAP XR 489 600 1 600 104 104 1427 1 21 22 100 480 HSAVK10 209368 Oct. 16, 1997 Uni-ZAP XR 490 1242 1 1242 131 131 1428 1 32 33 40 481 HSAWD74 209126 Jun. 19, 1997 Uni-ZAP XR 491 970 106 970 142 142 1429 1 26 27 142 481 HSAWD74 209126 Jun. 19, 1997 Uni-ZAP XR 861 646 1 646 122 122 1799 1 29 30 45 482 HSAWZ41 209463 Nov. 14, 1997 Uni-ZAP XR 492 1388 1 1388 98 98 1430 1 24 25 57 483 HSAXA83 209324 Oct. 02, 1997 Uni-ZAP XR 493 649 1 649 92 92 1431 1 22 23 74 484 HSAYB43 209568 Jan. 06, 1998 Uni-ZAP XR 494 1699 37 1699 89 89 1432 1 14 15 45 485 HSAYM40 209139 Jul. 03, 1997 Uni-ZAP XR 495 433 1 433 190 190 1433 1 19 20 63 486 HSDAJ46 209746 Apr. 07, 1998 Uni-ZAP XR 496 1537 92 1537 299 299 1434 1 18 19 262 487 HSDEK49 209603 Jan. 29, 1998 Uni-ZAP XR 497 1782 1 1782 60 60 1435 1 19 20 399 487 HSDEK49 209603 Jan. 29, 1998 Uni-ZAP XR 862 1590 96 1590 126 126 1800 1 21 22 305 488 HSDER95 209683 Mar. 20, 1998 Uni-ZAP XR 498 574 1 574 72 72 1436 1 25 26 71 489 HSDEZ20 209852 May 07, 1998 Uni-ZAP XR 499 795 1 795 58 58 1437 1 41 42 122 489 HSDEZ20 209852 May 07, 1998 Uni-ZAP XR 863 1540 1 1540 66 66 1801 1 41 42 97 490 HSDFW45 209551 Dec. 12, 1997 Uni-ZAP XR 500 1742 1 1742 118 118 1438 1 19 20 70 491 HSDJA15 203081 Jul. 30, 1998 Uni-ZAP XR 501 1443 1 1443 247 247 1439 1 20 21 152 492 HSDJJ82 209126 Jun. 19, 1997 Uni-ZAP XR 502 462 1 462 79 79 1440 1 32 33 52 493 HSDJL42 PTA-884 Uni-ZAP XR 503 2541 1 2523 84 84 1441 1 33 34 217 Oct. 28, 1999 493 HSDJL42 PTA-884 Uni-ZAP XR 864 2467 1 2467 27 27 1802 1 35 36 219 Oct. 28, 1999 493 HSDJL42 PTA-884 Uni-ZAP XR 865 2541 1 2523 78 78 1803 1 35 36 219 Oct. 28, 1999 494 HSDJM31 209148 Jul. 17, 1997 Uni-ZAP XR 504 561 1 561 351 351 1442 1 25 26 40 495 HSDSB09 209145 Jul. 17, 1997 pBLUESCRIPT ™ 505 809 1 809 16 16 1443 1 17 18 135 495 HSDSB09 209145 Jul. 17, 1997 pBLUESCRIPT ™ 866 819 1 819 22 22 1804 1 17 18 121 496 HSDSE75 209324 Oct. 02, 1997 pBLUESCRIPT ™ 506 1151 1 1151 160 160 1444 1 18 19 181 497 HSDZR57 209641 Feb. 25, 1998 pBLUESCRIPT ™ 507 308 1 308 27 27 1445 1 27 28 61 498 HSHAX21 209853 May 07, 1998 Uni-ZAP XR 508 1986 1 1986 177 177 1446 1 13 14 72 499 HSIAS17 209226 Aug. 28, 1997 Uni-ZAP XR 509 1781 1 1781 431 431 1447 1 22 23 257 499 HSIAS17 209226 Aug. 28, 1997 Uni-ZAP XR 867 1448 1 1224 108 108 1805 1 23 24 218 500 HSICV24 209580 Jan. 14, 1998 Uni-ZAP XR 510 1410 1 1410 117 117 1448 1 16 17 256 500 HSICV24 209580 Jan. 14, 1998 Uni-ZAP XR 868 1450 1 1450 150 150 1806 1 15 16 58 501 HSIDJ81 209551 Dec. 12, 1997 Uni-ZAP XR 511 1303 1 1303 8 8 1449 1 22 23 58 502 HSIDX71 PTA-843 Uni-ZAP XR 512 2118 1 2118 200 200 1450 1 41 42 59 Oct. 13, 1999 502 HSIDX71 PTA-843 Uni-ZAP XR 869 1868 1 1868 200 200 1807 1 41 42 59 Oct. 13, 1999 503 HSJBQ79 97924 Mar. 07, 1997 Uni-ZAP XR 513 587 1 587 41 41 1452 1 23 24 182 503 HSJBQ79 97924 Mar. 07, 1997 Uni-ZAP XR 870 1507 164 608 57 57 1808 1 19 20 327 503 HSJBQ79 97924 Mar. 07, 1997 Uni-ZAP XR 871 586 4 586 35 35 1809 1 23 24 184 504 HSKCP69 209009 Apr. 28, 1997 Uni-ZAP XR 514 1251 219 1120 49 49 1453 1 27 28 286 504 HSKCP69 209009 Apr. 28, 1997 Uni-ZAP XR 872 1250 223 1250 393 393 1810 1 31 32 171 505 HSKDA27 PTA-322 Uni-ZAP XR 515 4412 1 4412 786 786 1453 1 24 25 950 Jul. 09, 1999 505 HSKDA27 PTA-322 Uni-ZAP XR 873 1792 134 1792 127 127 1811 1 21 22 509 Jul. 09, 1999 505 HSKDA27 PTA-322 Uni-ZAP XR 874 1673 1 1673 12 12 1812 1 21 22 554 Jul. 09, 1999 506 HSKHZ81 209346 Oct. 09, 1997 pBLUESCRIPT ™ 516 969 1 969 64 64 1454 1 27 28 247 506 HSKHZ81 209346 Oct. 09, 1997 pBLUESCRIPT ™ 875 988 1 967 57 57 1813 1 27 28 247 507 HSKNB56 209346 Oct. 09, 1997 pBLUESCRIPT ™ 517 1334 449 1334 484 484 1455 1 25 26 85 508 HSLCQ82 209551 Dec. 12, 1997 Uni-ZAP XR 518 1476 1 1476 226 226 1456 1 28 29 84 508 HSLCQ82 209551 Dec. 12, 1997 Uni-ZAP XR 876 1501 1 1501 233 233 1814 1 22 23 57 509 HSLJG37 PTA-855 Uni-ZAP XR 519 2126 1 2126 114 114 1457 1 16 17 42 Oct. 18, 1999 509 HSLJG37 PTA-855 Uni-ZAP XR 877 1083 1 1083 206 206 1815 1 16 17 42 Oct. 18, 1999 509 HSLJG37 PTA-855 Uni-ZAP XR 878 1904 1 1904 1331 1816 1 6 Oct. 18, 1999 510 HSODE04 PTA-855 Uni-ZAP XR 520 1370 1 1370 202 202 1458 1 20 21 41 Oct. 18, 1999 510 HSODE04 PTA-855 Uni-ZAP XR 879 1937 1 1937 300 300 1817 1 20 21 41 Oct. 18, 1999 511 HSPBF70 203105 Aug. 13, 1998 pSport1 521 1397 288 1397 429 429 1459 1 19 20 97 512 HSQEO84 97974 Apr. 04, 1997 Uni-ZAP XR 522 931 1 931 87 87 1460 1 20 21 218 209080 May 29, 1997 512 HSQEO84 97974 Apr. 04, 1997 Uni-ZAP XR 880 971 13 971 91 91 1818 1 19 20 218 209080 May 29, 1997 512 HSQEO84 97974 Apr. 04, 1997 Uni-ZAP XR 881 968 8 968 86 86 1819 1 20 21 56 209080 May 29, 1997 513 HSSAJ29 209626 Feb. 12, 1998 Uni-ZAP XR 523 1044 1 1044 103 103 1461 1 25 26 47 514 HSSDX51 209683 Mar. 20, 1998 Uni-ZAP XR 524 1143 1 1143 133 133 1462 1 20 21 50 515 HSSFT08 209551 Dec. 12, 1997 Uni-ZAP XR 525 791 1 791 125 125 1463 1 34 35 58 516 HSSGD52 PTA-1543 Uni-ZAP XR 526 2425 1 2425 344 344 1464 1 32 33 606 Mar. 21, 2000 516 HSSGD52 PTA-1543 Uni-ZAP XR 882 2460 105 2460 338 338 1820 1 27 28 606 Mar. 21, 2000 517 HSSGG82 209580 Jan. 14, 1998 Uni-ZAP XR 527 1543 186 1543 203 203 1465 1 17 18 62 518 HSSJC35 209853 May 07, 1998 Uni-ZAP XR 528 1174 1 1174 62 62 1466 1 28 29 295 518 HSSJC35 209853 May 07, 1998 Uni-ZAP XR 883 1163 1 1163 55 55 1821 1 30 31 295 518 HSSJC35 209853 May 07, 1998 Uni-ZAP XR 884 1183 1 1183 66 66 1822 1 30 31 37 519 HSTBJ86 203027 Jun. 26, 1998 Uni-ZAP XR 529 1766 1 1766 120 120 1467 1 24 25 83 520 HSUBW09 209007 Apr. 28, 1997 Uni-ZAP XR 530 1021 1 1021 153 153 1468 1 31 32 56 209083 May 29, 1997 521 HSVAM10 209244 Sep. 12, 1997 Uni-ZAP XR 531 433 1 433 46 46 1469 1 27 28 51 522 HSVAT68 209641 Feb. 25, 1998 Uni-ZAP XR 532 1155 1 1155 63 63 1470 1 25 26 88 523 HSVBU91 209603 Jan. 29, 1998 Uni-ZAP XR 533 727 1 727 256 256 1471 1 18 19 90 524 HSXCG83 203570 Jan. 11, 1999 Uni-ZAP XR 534 2112 233 1573 101 101 1472 1 45 46 267 524 HSXCG83 203570 Jan. 11, 1999 Uni-ZAP XR 885 1938 58 1399 211 211 1823 1 22 23 172 525 HSXEQ06 PTA-847 Uni-ZAP XR 535 1598 1 1598 123 123 1473 1 24 25 60 f. 13, 1999 525 HSXEQ06 PTA-847 Uni-ZAP XR 886 768 21 768 136 136 1824 1 24 25 60 Oct. 13, 1999 525 HSXEQ06 PTA-847 Uni-ZAP XR 887 1392 1 1392 1271 1825 1 9 10 17 Oct. 13, 1999 526 HSXGI47 PTA-499 Uni-ZAP XR 536 1256 1 1256 87 87 1474 1 21 22 57 Aug. 11, 1999 527 HSYAV50 PTA-1544 pCMVSport 3.0 537 2801 1 2801 155 155 1475 1 23 24 672 Mar. 21, 2000 528 HSYAV66 209746 Apr. 07, 1998 pCMVSport 3.0 538 1407 1 1407 186 186 1476 1 28 29 69 529 HSYAZ50 PTA-849 pCMVSport 3.0 539 1097 1 1097 131 131 1477 1 18 19 56 Oct. 13, 1999 529 HSYAZ50 PTA-849 pCMVSport 3.0 888 768 226 768 345 345 1826 1 18 19 56 Oct. 13, 1999 529 HSYAZ50 PTA-849 pCMVSport 3.0 889 2087 770 875 723 1827 1 1 2 106 Oct. 13, 1999 529 HSYAZ50 PTA-849 pCMVSport 3.0 890 2096 1767 2050 2 1828 1 1 2 279 Oct. 13, 1999 530 HSYAZ63 PTA-163 pCMVSport 3.0 540 3466 1655 3347 448 448 1478 1 30 31 434 Jun. 01, 1999 530 HSYAZ63 PTA-163 pCMVSport 3.0 891 1707 1 1707 215 215 1829 1 21 22 40 Jun. 01, 1999 531 HSYBG37 209463 Nov. 14, 1997 pCMVSport 3.0 541 1238 1 1238 47 47 1479 1 24 25 305 531 HSYBG37 209463 Nov. 14, 1997 pCMVSport 3.0 892 1239 1 1239 48 48 1830 1 24 25 305 532 HSZAF47 209124 Jun. 19, 1997 Uni-ZAP XR 542 1304 1 1304 106 106 1480 1 16 17 289 532 HSZAF47 209124 Jun. 19, 1997 Uni-ZAP XR 893 1333 2 1333 107 107 1831 1 18 19 127 533 HT3SF53 PTA-499 Uni-ZAP XR 543 1926 1 1926 184 184 1481 1 27 28 68 Aug. 11, 1999 534 HT5GJ57 209889 May 22, 1998 Uni-ZAP XR 544 1773 1 1773 105 105 1482 1 25 26 243 534 HT5GJ57 209889 May 22, 1998 Uni-ZAP XR 894 1797 92 1797 122 122 1832 1 25 26 190 535 HTADW91 PTA-1543 Uni-ZAP XR 545 1481 54 1481 59 59 1483 1 32 33 364 Mar. 21, 2000 536 HTADX17 209124 Jun. 19, 1997 Uni-ZAP XR 546 1147 0 1148 92 92 1484 1 23 24 142 536 HTADX17 209124 Jun. 19, 1997 Uni-ZAP XR 895 1140 22 1140 84 84 1833 1 19 20 142 537 HTAEE28 PTA-843 Uni-ZAP XR 547 1341 1 1341 319 319 1485 1 33 34 282 Oct. 13, 1999 537 HTAEE28 PTA-843 Uni-ZAP XR 896 738 159 738 372 372 1834 1 33 34 122 Oct. 13, 1999 537 HTAEE28 PTA-843 Uni-ZAP XR 897 935 1 807 124 1835 1 1 2 216 Oct. 13, 1999 538 HTDAF28 97974 Apr. 04, 1997 pSport1 548 912 1 912 38 38 1486 1 22 23 87 209080 May 29, 1997 539 HTEAF65 PTA-322 Uni-ZAP XR 549 563 1 563 135 135 1487 1 19 20 75 Jul. 09, 1999 540 HTEBI28 209177 Jul. 24, 1997 Uni-ZAP XR 550 413 1 413 43 43 1488 1 20 21 67 541 HTEDF80 209511 Dec. 03, 1997 Uni-ZAP XR 551 1306 1 1306 696 696 1489 1 21 22 126 542 HTEDY42 209241 Sep. 12, 1997 Uni-ZAP XR 552 754 1 754 19 19 1490 1 23 24 233 542 HTEDY42 209241 Sep. 12, 1997 Uni-ZAP XR 898 810 1 810 19 19 1836 1 23 24 77 543 HTEFU65 209324 Oct. 02, 1997 Uni-ZAP XR 553 1028 1 1028 231 231 1491 1 24 25 46 544 HTEGA76 97958 Mar. 13, 1997 Uni-ZAP XR 554 450 1 450 90 90 1492 1 43 44 65 209072 May 22, 1997 545 HTEGI42 PTA-842 Uni-ZAP XR 555 978 1 978 26 26 1493 1 19 20 257 Oct. 13, 1999 545 HTEGI42 PTA-842 Uni-ZAP XR 899 1092 1 1092 145 145 1837 1 19 20 257 Oct. 13, 1999 545 HTEGI42 PTA-842 Uni-ZAP XR 900 284 1 133 1 1838 1 1 2 94 Oct. 13, 1999 545 HTEGI42 PTA-842 Uni-ZAP XR 901 1494 754 937 1081 1839 1 1 2 82 Oct. 13, 1999 545 HTEGI42 PTA-842 Uni-ZAP XR 902 1014 1 806 670 1840 1 1 2 60 Oct. 13, 1999 546 HTEHR24 209224 Aug. 28, 1997 Uni-ZAP XR 556 1075 50 1075 84 84 1494 1 29 30 163 546 HTEHR24 209224 Aug. 28, 1997 Uni-ZAP XR 903 1038 1 1038 41 41 1841 1 28 29 124 547 HTEHU93 209090 Jun. 05, 1997 Uni-ZAP XR 557 738 1 738 188 188 1495 1 24 25 142 547 HTEHU93 209090 Jun. 05, 1997 Uni-ZAP XR 904 745 1 745 187 187 1842 1 24 25 113 548 HTEIP36 209244 Sep. 12, 1997 Uni-ZAP XR 558 752 1 752 22 22 1496 1 19 20 58 549 HTEIV80 209511 Dec. 03, 1997 Uni-ZAP XR 559 1748 1 1748 203 203 1497 1 14 15 47 550 HTEJN13 97958 Mar. 13, 1997 Uni-ZAP XR 560 1094 1 1094 156 156 1498 1 15 16 208 209072 May 22, 1997 550 HTEJN13 97958 Mar. 13, 1997 Uni-ZAP XR 905 1147 1 1147 163 163 1843 1 15 16 159 209072 May 22, 1997 550 HTEJN13 97958 Mar. 13, 1997 Uni-ZAP XR 906 1134 1 1134 155 155 1844 1 19 20 71 209072 May 22, 1997 551 HTELM16 203648 Feb. 09, 1999 Uni-ZAP XR 561 531 1 531 121 121 1499 1 21 22 84 552 HTEPG70 203570 Jan. 11, 1999 Uni-ZAP XR 562 813 1 813 365 365 1500 1 27 28 89 553 HTGAU75 209563 Dec. 18, 1997 Uni-ZAP XR 563 1713 1 1713 149 149 1501 1 33 34 142 554 HTGEP89 97977 Apr. 04, 1997 Uni-ZAP XR 564 703 1 703 285 285 1502 1 29 30 94 209082 May 29, 1997 555 HTHBG43 PTA-843 Uni-ZAP XR 565 848 1 848 47 47 1503 1 39 Oct. 13, 1999 555 HTHBG43 PTA-843 Uni-ZAP XR 907 632 103 632 149 149 1845 1 39 Oct. 13, 1999 556 HTHCA18 PTA-844 Uni-ZAP XR 566 1818 1 1818 231 231 1504 1 15 16 38 Oct. 13, 1999 556 HTHCA18 PTA-844 Uni-ZAP XR 908 2036 1 2036 224 224 1846 1 15 16 38 Oct. 13, 1999 557 HTHDJ94 209746 Apr. 07, 1998 Uni-ZAP XR 567 1632 20 1632 66 66 1505 1 26 27 292 558 HTHDS25 203071 Jul. 27, 1998 Uni-ZAP XR 568 1061 1 1061 70 70 1506 1 15 16 90 559 HTJMA95 209853 May 07, 1998 pCMVSport 2.0 569 1650 198 1569 527 527 1507 1 22 23 181 560 HTJML75 PTA-868 pCMVSport 2.0 570 2762 1 2762 30 30 1508 1 1 2 822 Oct. 26, 1999 560 HTJML75 PTA-868 pCMVSport 2.0 909 2694 21 2694 335 1847 1 20 21 64 Oct. 26, 1999 561 HTLAA40 209241 Sep. 12, 1997 Uni-ZAP XR 571 956 1 956 33 33 1509 1 28 29 71 562 HTLBE23 PTA-842 Uni-ZAP XR 572 1216 1 1216 129 129 1510 1 17 18 45 Oct. 13, 1999 562 HTLBE23 PTA-842 Uni-ZAP XR 910 810 286 810 205 1848 1 5 Oct. 13, 1999 563 HTLEP53 209641 Feb. 25, 1998 Uni-ZAP XR 573 818 1 818 73 73 1511 1 43 44 101 564 HTLFE42 209138 Jul. 03, 1997 Uni-ZAP XR 574 712 1 712 116 116 1512 1 22 23 77 565 HTLFE57 PTA-1543 Uni-ZAP XR 575 2248 1 2248 124 124 1513 1 17 18 188 Mar. 21, 2000 565 HTLFE57 PTA-1543 Uni-ZAP XR 911 2298 1157 2214 189 189 1849 1 18 19 170 Mar. 21, 2000 565 HTLFE57 PTA-1543 Uni-ZAP XR 912 928 1 928 110 110 1850 1 18 19 170 Mar. 21, 2000 566 HTLGE31 PTA-2081 Uni-ZAP XR 576 534 1 534 51 51 1514 1 17 18 86 Jun. 09, 2000 567 HTLHY14 203648 Feb. 09, 1999 Uni-ZAP XR 577 1032 1 1032 36 36 1515 1 17 18 246 568 HTLIT32 203570 Jan. 11, 1999 Uni-ZAP XR 578 1074 164 897 288 288 1516 1 26 27 246 569 HTLIV19 PTA-2081 Uni-ZAP XR 579 978 1 978 110 110 1517 1 33 34 84 Jun. 09, 2000 570 HTNBO91 209241 Sep. 12, 1997 pBLUESCRIPT ™ 580 300 1 300 7 7 1518 1 26 27 40 SK− 571 HTOAK16 209368 Oct. 16, 1997 Uni-ZAP XR 581 1466 1 1466 87 87 1519 1 18 19 110 572 HTODK73 209244 Sep. 12, 1997 Uni-ZAP XR 582 1019 4 1019 43 43 1520 1 23 24 59 573 HTODO72 209299 Sep. 25, 1997 Uni-ZAP XR 583 973 1 973 183 183 1521 1 16 17 24 574 HTOGR42 209603 Jan. 29, 1998 Uni-ZAP XR 584 1430 1 1430 14 14 1522 1 18 19 56 574 HTOGR42 209603 Jan. 29, 1998 Uni-ZAP XR 913 1433 1 1433 13 13 1851 1 18 19 60 575 HTOHM15 PTA-843 Uni-ZAP XR 585 1949 1 1949 30 30 1523 1 20 21 61 Oct. 13, 1999 575 HTOHM15 PTA-843 Uni-ZAP XR 914 408 1 408 23 23 1852 1 20 21 61 Oct. 13, 1999 575 HTOHM15 PTA-843 Uni-ZAP XR 915 1299 982 1274 71 1853 1 1 2 322 Oct. 13, 1999 575 HTOHM15 PTA-843 Uni-ZAP XR 916 1669 1 1622 1555 1854 1 9 10 13 Oct. 13, 1999 576 HTOHT18 209745 Apr. 07, 1998 Uni-ZAP XR 586 1499 267 1499 433 433 1524 1 24 25 53 577 HTOIY21 209852 May 07, 1998 Uni-ZAP XR 587 1558 1 1558 91 91 1525 1 14 15 231 578 HTOIZ02 PTA-843 Uni-ZAP XR 588 549 1 549 243 243 1526 1 16 17 50 Oct. 13, 1999 578 HTOIZ02 PTA-843 Uni-ZAP XR 917 1369 746 1345 2 1855 1 1 2 240 Oct. 13, 1999 579 HTOJA73 203105 Aug. 13, 1998 Uni-ZAP XR 589 1294 1 1294 100 100 1527 1 21 22 41 580 HTOJK60 209324 Oct. 02, 1997 Uni-ZAP XR 590 904 1 904 217 217 1528 1 18 19 32 581 HTPBW79 209511 Dec. 03, 1997 Uni-ZAP XR 591 1374 1 1374 178 178 1529 1 22 23 362 581 HTPBW79 209511 Dec. 03, 1997 Uni-ZAP XR 918 1515 118 1507 302 302 1856 1 24 25 362 581 HTPBW79 209511 Dec. 03, 1997 Uni-ZAP XR 919 1404 1 1404 92 92 1857 1 22 23 415 582 HTSEW17 209138 Jul. 03, 1997 pBLUESCRIPT ™ 592 652 1 652 170 170 1530 1 34 35 37 583 HTTDB46 203484 Nov. 17, 1998 Uni-ZAP XR 593 3059 1 3059 55 55 1531 1 17 18 318 583 HTTDB46 203484 Nov. 17, 1998 Uni-ZAP XR 920 2008 215 2008 153 153 1858 1 17 18 461 584 HTWCT03 209086 May 29, 1997 pSport1 594 1963 1 1963 334 334 1532 1 26 27 101 585 HTWDF76 209852 May 07, 1998 pSport1 595 963 1 963 316 316 1533 1 24 25 85 586 HTXAJ12 209423 Oct. 30, 1997 Uni-ZAP XR 596 675 1 675 91 91 1534 1 18 19 111 586 HTXAJ12 209423 Oct. 30, 1997 Uni-ZAP XR 921 675 1 675 91 91 1859 1 18 19 111 587 HTXCV12 209423 Oct. 30, 1997 Uni-ZAP XR 597 1134 1 1134 175 175 1535 1 27 28 102 587 HTXCV12 209423 Oct. 30, 1997 Uni-ZAP XR 922 1162 1 1162 183 183 1860 1 27 28 91 588 HTXDW56 209746 Apr. 07, 1998 Uni-ZAP XR 598 1583 1 1583 217 217 1536 1 21 22 201 589 HTXFL30 209603 Jan. 29, 1998 Uni-ZAP XR 599 1991 1 1991 30 30 1537 1 39 40 102 590 HTXKF95 PTA-622 Uni-ZAP XR 600 975 170 966 421 421 1538 1 28 29 78 Sep. 02, 1999 590 HTXKF95 PTA-622 Uni-ZAP XR 923 884 79 875 330 330 1861 1 28 29 78 Sep. 02, 1999 591 HTXKP61 203364 Oct. 19, 1998 Uni-ZAP XR 601 1209 1 1209 169 169 1539 1 33 34 42 592 HUDBZ89 209407 Oct. 23, 1997 ZAP Express 602 2135 1 2135 1085 1085 1540 1 17 18 73 592 HUDBZ89 209407 Oct. 23, 1997 ZAP Express 924 1265 1 1265 197 197 1862 1 17 18 54 593 HUFBY15 PTA-1543 pSport1 603 1193 1 1193 49 49 1541 1 26 27 159 Mar. 21, 2000 593 HUFBY15 PTA-1543 pSport1 925 1012 1 1012 74 74 1863 1 26 27 145 Mar. 21, 2000 594 HUFEF62 209852 May 07, 1998 pSport1 604 518 1 518 190 190 1542 1 28 29 68 594 HUFEF62 209852 May 07, 1998 pSport1 926 539 1 539 182 182 1864 1 28 29 68 595 HUKAH51 209568 Jan. 06, 1998 Lambda ZAP II 605 853 1 853 286 286 1543 1 20 21 151 595 HUKAH51 209568 Jan. 06, 1998 Lambda ZAP II 927 754 1 754 144 144 1865 1 22 23 142 595 HUKAH51 209568 Jan. 06, 1998 Lambda ZAP II 928 667 1 667 55 55 1866 1 22 23 119 596 HUKBT29 209746 Apr. 07, 1998 Lambda ZAP II 606 1757 56 1757 74 74 1544 1 19 20 506 597 HUSIG64 209423 Oct. 30, 1997 pSport1 607 1010 1 1010 9 9 1545 1 21 22 334 598 HUSXS50 209651 Mar. 04, 1998 pSport1 608 2561 1 2561 280 280 1546 1 19 20 522 598 HUSXS50 209651 Mar. 04, 1998 pSport1 929 2025 1098 1997 281 281 1867 1 30 31 462 598 HUSXS50 209651 Mar. 04, 1998 pSport1 930 1020 1 1020 179 179 1868 1 23 24 174 599 HVARW53 PTA-2076 pSport1 609 1015 1 1015 111 111 1547 1 34 35 186 Jun. 09, 2000 599 HVARW53 PTA-2076 pSport1 931 1006 1 1006 96 96 1869 1 34 35 164 Jun. 09, 2000 600 HWAAD63 203570 Jan. 11, 1999 pCMVSport 3.0 610 3308 1 3308 322 322 1548 1 30 31 168 600 HWAAD63 203570 Jan. 11, 1999 pCMVSport 3.0 932 3306 1 3306 322 322 1870 1 30 31 53 600 HWAAD63 203570 Jan. 11, 1999 pCMVSport 3.0 933 2194 1 2194 312 312 1871 1 30 31 169 601 HWABA81 209463 Nov. 14, 1997 pCMVSport 3.0 611 866 1 866 57 57 1549 1 21 22 48 602 HWABY10 203071 Jul. 27, 1998 pCMVSport 3.0 612 2950 78 2914 263 263 1550 1 22 23 168 603 HWADJ89 PTA-1543 pCMVSport 3.0 613 1769 529 1769 581 581 1551 1 1 2 43 Mar. 21, 2000 604 HWBAO62 209603 Jan. 29, 1998 pCMVSport 3.0 614 1903 1 1903 52 52 1552 1 30 31 212 604 HWBAO62 209603 Jan. 29, 1998 pCMVSport 3.0 934 1940 1 1940 81 81 1872 1 30 31 101 605 HWBAR88 PTA-867 pCMVSport 3.0 615 1051 1 1051 156 156 1553 1 18 19 75 Oct. 26, 1999 606 HWBCB89 PTA-499 pCMVSport 3.0 616 1317 3 1317 37 37 1554 1 19 20 187 Aug. 11, 1999 606 HWBCB89 PTA-499 pCMVSport 3.0 935 1315 1 1315 35 35 1873 1 19 20 187 Aug. 11, 1999 607 HWBCP79 209641 Feb. 25, 1998 pCMVSport 3.0 617 1138 1 1138 243 243 1555 1 21 22 105 607 HWBCP79 209641 Feb. 25, 1998 pCMVSport 3.0 936 1138 1 1138 233 233 1874 1 21 22 105 608 HWBDP28 209641 Feb. 25, 1998 pCMVSport 3.0 618 1841 1 1841 1342 1342 1556 1 25 26 67 608 HWBDP28 209641 Feb. 25, 1998 pCMVSport 3.0 937 314 1 314 132 132 1875 1 25 26 61 609 HWBFE57 PTA-868 pCMVSport 3.0 619 1133 36 1133 227 227 1557 1 36 37 302 Oct. 26, 1999 609 HWBFE57 PTA-868 pCMVSport 3.0 938 5811 3302 5811 3300 1876 1 16 17 37 Oct. 26, 1999 609 HWBFE57 PTA-868 pCMVSport 3.0 939 1012 1 1012 622 1877 1 10 11 16 Oct. 26, 1999 610 HWDAC39 209641 Feb. 25, 1998 pCMVSport 3.0 620 753 1 753 96 96 1558 1 20 21 110 610 HWDAC39 209641 Feb. 25, 1998 pCMVSport 3.0 940 734 1 734 85 85 1878 1 20 21 117 611 HWDAH38 PTA-868 pCMVSport 3.0 621 1604 1 1604 255 255 1559 1 20 21 40 Oct. 26, 1999 611 HWDAH38 PTA-868 pCMVSport 3.0 941 796 1 796 319 319 1879 1 20 21 40 Oct. 26, 1999 612 HWHGP71 203858 Mar. 18, 1999 pCMVSport 3.0 622 1021 1 1021 389 389 1560 1 51 52 211 612 HWHGP71 203858 Mar. 18, 1999 pCMVSport 3.0 942 1037 1 1037 394 394 1880 1 18 19 77 613 HWHGQ49 209641 Feb. 25, 1998 pCMVSport 3.0 623 985 1 985 511 511 1561 1 17 18 90 613 HWHGQ49 209641 Feb. 25, 1998 pCMVSport 3.0 943 1410 33 1410 306 306 1881 1 22 23 150 614 HWHGU54 209782 Apr. 20, 1998 pCMVSport 3.0 624 1445 1 1445 145 145 1562 1 19 20 414 615 HWHGZ51 PTA-499 pCMVSport 3.0 625 1699 1 1699 33 33 1563 1 30 31 346 Aug. 11, 1999 616 HWHHL34 203181 Sep. 09, 1998 pCMVSport 3.0 626 1529 95 1529 131 131 1564 1 30 31 188 616 HWHHL34 203181 Sep. 09, 1998 pCMVSport 3.0 944 1796 1 1796 209 209 1882 1 31 32 102 616 HWHHL34 203181 Sep. 09, 1998 pCMVSport 3.0 945 2136 1 2136 101 101 1883 1 30 31 188 617 HWLEV32 PTA-884 pSport1 627 1218 1 1218 39 39 1565 1 18 19 45 Oct. 28, 1999 617 HWLEV32 PTA-884 pSport1 946 1203 1 1203 29 29 1884 1 18 19 45 Oct. 28, 1999 617 HWLEV32 PTA-884 pSport1 947 1144 528 596 3 1885 1 1 2 136 Oct. 28, 1999 617 HWLEV32 PTA-884 pSport1 948 1120 791 851 1 1886 1 1 2 141 Oct. 28, 1999 618 HWLIH65 203081 Jul. 30, 1998 pSport1 628 831 1 831 129 129 1566 1 18 19 165 619 HWTBK81 209138 Jul. 03, 1997 Uni-ZAP XR 629 637 78 635 139 139 1567 1 23 24 155 620 HYAAJ71 203517 Dec. 10, 1998 pCMVSport 3.0 630 3337 1 3337 190 190 1568 1 31 32 62 621 HUSBA88 PTA-623 Lambda ZAP II 631 2733 27 2733 270 270 1569 1 15 16 615 Sep. 02, 1999 Table 1B (Comprised of Tables 1B.1 and 1B.2)

The first column in Table 1B.1 and Table 1B.2 provides the gene number in the application corresponding to the clone identifier. The second column in Table 1B.1 and Table 1B.2 provides a unique “Clone ID:” for the cDNA clone related to each contig sequence disclosed in Table 1B.1 and Table 1B.2. This clone ID references the cDNA clone which contains at least the 5′ most sequence of the assembled contig and at least a portion of SEQ ID NO:X as determined by directly sequencing the referenced clone. The referenced clone may have more sequence than described in the sequence listing or the clone may have less. In the vast majority of cases, however, the clone is believed to encode a full-length polypeptide. In the case where a clone is not full-length, a full-length cDNA can be obtained by methods described elsewhere herein. The third column in Table 1B.1 and Table 1B.2 provides a unique “Contig ID” identification for each contig sequence. The fourth column in Table 1B.1 and Table 1B.2 provides the “SEQ ID NO:” identifier for each of the contig polynucleotide sequences disclosed in Table 1B.

Table 1B.1

The fifth column in Table 1B.1, “ORF (From-To)”, provides the location (i.e., nucleotide position numbers) within the polynucleotide sequence “SEQ ID NO:X” that delineate the preferred open reading frame (ORF) shown in the sequence listing and referenced in Table 1B.1, column 6, as SEQ ID NO:Y. Where the nucleotide position number “To” is lower than the nucleotide position number “From”, the preferred ORF is the reverse complement of the referenced polynucleotide sequence. The sixth column in Table 1B.1 provides the corresponding SEQ ID NO:Y for the polypeptide sequence encoded by the preferred ORF delineated in column 5. In one embodiment, the invention provides an amino acid sequence comprising, or alternatively consisting of, a polypeptide encoded by the portion of SEQ ID NO:X delineated by “ORF (From-To)”. Also provided are polynucleotides encoding such amino acid sequences and the complementary strand thereto. Column 7 in Table 1B.1 lists residues comprising epitopes contained in the polypeptides encoded by the preferred ORF (SEQ ID NO:Y), as predicted using the algorithm of Jameson and Wolf, (1988) Comp. Appl. Biosci. 4:181-186. The Jameson-Wolf antigenic analysis was performed using the computer program PROTEAN (Version 3.11 for the Power MacIntosh, DNASTAR, Inc., 1228 South Park Street Madison, Wis.). In specific embodiments, polypeptides of the invention comprise, or alternatively consist of, at least one, two, three, four, five or more of the predicted epitopes as described in Table 1B. It will be appreciated that depending on the analytical criteria used to predict antigenic determinants, the exact address of the determinant may vary slightly.

Column 8 in Table 1B.1 provides a chromosomal map location for certain polynucleotides of the invention. Chromosomal location was determined by finding exact matches to EST and cDNA sequences contained in the NCBI (National Center for Biotechnology Information) UniGene database. Each sequence in the UniGene database is assigned to a “cluster”; all of the ESTs, cDNAs, and STSs in a cluster are believed to be derived from a single gene. Chromosomal mapping data is often available for one or more sequence(s) in a UniGene cluster; this data (if consistent) is then applied to the cluster as a whole. Thus, it is possible to infer the chromosomal location of a new polynucleotide sequence by determining its identity with a mapped UniGene cluster.

A modified version of the computer program BLASTN (Altshul, et al., J. Mol. Biol. 215:403-410 (1990), and Gish, and States, Nat. Genet. 3:266-272) (1993) was used to search the UniGene database for EST or cDNA sequences that contain exact or near-exact matches to a polynucleotide sequence of the invention (the ‘Query’). A sequence from the UniGene database (the ‘Subject’) was said to be an exact match if it contained a segment of 50 nucleotides in length such that 48 of those nucleotides were in the same order as found in the Query sequence. If all of the matches that met this criteria were in the same UniGene cluster, and mapping data was available for this cluster, it is indicated in Table 1B under the heading “Cytologic Band”. Where a cluster had been further localized to a distinct cytologic band, that band is disclosed; where no banding information was available, but the gene had been localized to a single chromosome, the chromosome is disclosed.

Once a presumptive chromosomal location was determined for a polynucleotide of the invention, an associated disease locus was identified by comparison with a database of diseases which have been experimentally associated with genetic loci. The database used was the Morbid Map, derived from OMIM™ and National Center for Biotechnology Information, National Library of Medicine (Bethesda, Md.) 2000. If the putative chromosomal location of a polynucleotide of the invention (Query sequence) was associated with a disease in the Morbid Map database, an OMIM reference identification number was noted in column 9, Table 1B.1, labelled “OMIM Disease Reference(s). Table 5 is a key to the OMIM reference identification numbers (column 1), and provides a description of the associated disease in Column 2.

Table 1B.2

Column 5, in Table 1B.2, provides an expression profile and library code:count for each of the contig sequences (SEQ ID NO:X) disclosed in Table 1B, which can routinely be combined with the information provided in Table 4 and used to determine the tissues, cells, and/or cell line libraries which predominantly express the polynucleotides of the invention. The first number in Table 1B.2, column 5 (preceding the colon), represents the tissue/cell source identifier code corresponding to the code and description provided in Table 4. The second number in column 5 (following the colon) represents the number of times a sequence corresponding to the reference polynucleotide sequence was identified in the corresponding tissue/cell source. Those tissue/cell source identifier codes in which the first two letters are “AR” designate information generated using DNA array technology. Utilizing this technology, cDNAs were amplified by PCR and then transferred, in duplicate, onto the array. Gene expression was assayed through hybridization of first strand cDNA probes to the DNA array. cDNA probes were generated from total RNA extracted from a variety of different tissues and cell lines. Probe synthesis was performed in the presence of ³³P dCTP, using oligo (dT) to prime reverse transcription. After hybridization, high stringency washing conditions were employed to remove non-specific hybrids from the array. The remaining signal, emanating from each gene target, was measured using a Phosphorimager. Gene expression was reported as Phosphor Stimulating Luminescence (PSL) which reflects the level of phosphor signal generated from the probe hybridized to each of the gene targets represented on the array. A local background signal subtraction was performed before the total signal generated from each array was used to normalize gene expression between the different hybridizations. The value presented after “[array code]:” represents the mean of the duplicate values, following background subtraction and probe normalization. One of skill in the art could routinely use this information to identify normal and/or diseased tissue(s) which show a predominant expression pattern of the corresponding polynucleotide of the invention or to identify polynucleotides which show predominant and/or specific tissue and/or cell expression. LENGTHY TABLE REFERENCED HERE US20080103090A1-20080501-T00001 Please refer to the end of the specification for access instructions. LENGTHY TABLE REFERENCED HERE US20080103090A1-20080501-T00002 Please refer to the end of the specification for access instructions.

Table 1C summarizes additional polynucleotides encompassed by the invention (including cDNA clones related to the sequences (Clone ID:), contig sequences (contig identifier (Contig ID:) contig nucleotide sequence identifiers (SEQ ID NO:X)), and genomic sequences (SEQ ID NO:B). The first column provides a unique clone identifier, “Clone ID:”, for a cDNA clone related to each contig sequence. The second column provides the sequence identifier, “SEQ ID NO:X”, for each contig sequence. The third column provides a unique contig identifier, “Contig ID:” for each contig sequence. The fourth column, provides a BAC identifier “BAC ID NO:A” for the BAC clone referenced in the corresponding row of the table. The fifth column provides the nucleotide sequence identifier, “SEQ ID NO:B” for a fragment of the BAC clone identified in column four of the corresponding row of the table. The sixth column, “Exon From-To”, provides the location (i.e., nucleotide position numbers) within the polynucleotide sequence of SEQ ID NO:B which delineate certain polynucleotides of the invention that are also exemplary members of polynucleotide sequences that encode polypeptides of the invention (e.g., polypeptides containing amino acid sequences encoded by the polynucleotide sequences delineated in column six, and fragments and variants thereof). TABLE 1C SEQ ID SEQ ID cDNA Clone ID NO: X CONTIG ID: BAC ID: A NO: B EXONFrom-To HAGAN21 21 1026956 AC011967 1885 1-839 HAGAN21 21 1026956 AC074370 1886 1-839 HAGAN21 21 1026956 AL355151 1887 1-837 HAGAN21 21 1026956 AL121796 1888 1-836 HAGAN21 21 1026956 AC011967 1889 1-367372-11671180- 17913777-40784113- 4269 HAGAN21 21 1026956 AC074370 1890 1-366373-11671180- 17933779-40814117- 4273 HAGAN21 21 1026956 AL355151 1891 1-364373-11661179- 17903780-4082 HAGAN21 21 1026956 AL121796 1892 1-367374-11651178- 17913767-40694105- 4262 HAIBP89 31 727543 AC005214 1893 1-228817-3471 HAIBP89 31 727543 AC005214 1894 1-539 HBCPB32 56 1352403 AC024191 1895 1-6431421-16364917- 5536 HBCQL32 57 1134954 AC069250 1896 1-461504-10111964- 24242747-28593098- 32514239-6717 HBCQL32 57 1134954 AC069250 1897 1-418 HBINS58 62 1352386 AL096774 1898 1-10232010- 22392581-29623153- 32233324-34933973- 4126 HBINS58 62 1352386 AL096774 1899 1-341 HBINS58 62 1352386 AL096774 1900 1-142 HBMCI50 69 668268 AL139132 1901 1-890 HBMCI50 69 668268 AL359179 1902 1-891 HBMCI50 69 668268 AL139132 1903 1-155 HBMCI50 69 668268 AL359179 1904 1-155 HBOEG11 71 1300752 AL139352 1905 1-253438-5392336- 28014986-52095967- 64399014-94529829- 1008410404- 1050312165-13255 HBOEG11 71 1300752 AL139352 1906 1-559 HCEFB80 79 1143407 AL022327 1907 1-22713506- 36584643-48109039- 91649382-950910587- 1072011135- 1119511265- 1171614644- 1546617451- 1752618012- 1811420530- 2063220957- 2100923696- 2378525338- 2557525969-26166 HCEWE17 83 941941 AL139130 1908 1-170463-598623- 13461404-15232059- 21592350-26163068- 32543428-3878 HCOOS80 96 1134974 AC003688 1909 1-7181054-11581660- 19804003-40734364- 45164646-47494852- 49955121-52135354- 54245526-56695759- 58325850-61766756- 68297023-71757259- 73987531-77118134- 83818463- 1358513691- 1432314437-14918 HCOOS80 96 1134974 AC026954 1910 1-138273-453876- 11231205-4456 HCOOS80 96 1134974 AC003688 1911 1-125203-4801463- 16472048-20772229- 23232725-37843867- 4682 HCWGU37 103 1042325 AC007459 1912 1-242 HCWGU37 103 1042325 AC022435 1913 1-2185587-5754 HCWGU37 103 1042325 AC022051 1914 1-294 HCWGU37 103 1042325 AC023672 1915 1-196 HCWGU37 103 1042325 AC011101 1916 1-100 HCWGU37 103 1042325 AC034243 1917 1-3122334-2364 HCWGU37 103 1042325 AC010454 1918 1-2185588-5755 HCWGU37 103 1042325 AC026144 1919 1-183 HCWGU37 103 1042325 AC009691 1920 1-292 HCWGU37 103 1042325 AL354696 1921 1-181 HCWGU37 103 1042325 AC073219 1922 1-123 HCWGU37 103 1042325 AC027414 1923 1-270 HCWGU37 103 1042325 AC010454 1924 1-303 HDPWN93 140 992925 AC004590 1925 1-276489-591866- 9881106-12811323- 14441632-17991866- 20162109-23132634- 32053360-34723528- 37443820-50066580- 69197076-72768057- 81538318-8680 HDPWN93 140 992925 AC021491 1926 1-275488-590865- 9871105-12801322- 14431631-17981865- 20152108-23122633- 32043359-34713527- 37433819-50056579- 69187075-72758054- 81508315-8677 HDPWN93 140 992925 AC004590 1927 1-303727-12525721- 5846 HDPWN93 140 992925 AC021491 1928 1-303727-12535723- 5848 HDTEK44 146 1025421 AC022100 1929 1-2932 HDTEK44 146 1025421 AC022100 1930 1-353 HDTFE17 148 1043391 AF196972 1931 1-74391-5241481- 15361623-16992092- 24482537-26113085- 31793315-33956429- 65146997-74077611- 76938316-87749534- 96809770-987510373- 10876 HDTFE17 148 1043391 AF196972 1932 1-742 HDTMK50 151 1011485 AL354768 1933 1-1340 HDTMK50 151 1011485 AC012318 1934 1-147 HDTMK50 151 1011485 AL354768 1935 1-590 HE8QV67 162 1050076 AL133410 1936 1-7654403-44964696- 48135112-55845780- 58305850-77667774- 82848479-89028986- 91109305-94819658- 99449998- 1010610202- 1271812797- 1288612974- 1306313259- 1464514680- 1494115625- 1571415825- 1589515965- 1611416204-16772 HE8QV67 162 1050076 AL133410 1937 1-851082-19512761- 3118 HE8QV67 162 1050076 AL133410 1938 1-2628-267828- 39524173-48374930- 69557105-72307451- 76557842-79478245- 83298599-87568855- 89409219-93569728- 986110190-10231 HEBBN36 172 486120 AC005180 1939 1-341704-15591704- 30893146-41664768- 48715384-54855535- 61826595-7328 HEBBN36 172 486120 AC002557 1940 1-1387 HEBBN36 172 486120 AC002557 1941 1-856 HEBBN36 172 486120 AC002557 1942 1-971 HETLM70 193 1177512 AC012314 1943 1-43861-10311576- 17431924-21322203- 24322473-29053177- 33603651-43324422- 45834830-49955086- 5365 HETLM70 193 1177512 AC009968 1944 1-43857-10271570- 17371918-21262197- 24262467-28993171- 33543644-43264416- 45774824-49895080- 5360 HETLM70 193 1177512 AC012314 1945 1-1811281-14632719- 29833158-34113804- 63476745-68797118- 73197420-75217859- 83058552-86029988- 1033410415- 1077811003- 1112711210- 1130311334- 1183213093- 1314513703- 1383713918- 1415215415- 1551115613- 1574215998- 1608716231- 1630716447- 1721118520- 1879621777-22001 HETLM70 193 1177512 AC009968 1946 1-1801275-14572712- 29763150-34033796- 63326730-68647103- 73037404-75057843- 82898536-85869970- 1031210393- 1075610981- 1110511188- 1180513068- 1312013678- 1381213905-13994 HFIIZ70 202 1043350 AC005005 1947 1-3681579-2971 HFIIZ70 202 1043350 AC005005 1948 1-484517-11422842- 31763376-34933575- 37403873-42274728- 49355074-53515446- 55645772-59607287- 76277721-80978218- 932512098- 1216112780- 1326613482- 1366613748- 1381714445- 1451914595- 1492815658- 1575415848- 1592316016- 1611216512- 1666021313- 2144821710- 2187021899- 2247022634- 2278723169-23307 HFVGE32 215 854545 AL160269 1949 1-1122 HFVGE32 215 854545 AL138754 1950 1-1120 HHBCS39 232 1003028 AL390960 1951 1-2979 HHBCS39 232 1003028 AL358992 1952 1-2983 HHBCS39 232 1003028 AL358992 1953 1-207 HHEPD24 238 498227 AC025937 1954 1-216 HHGCM76 250 662329 AC003665 1955 1-70304-609900- 10901240-18352272- 24902581-3598 HHGCM76 250 662329 AC003665 1956 1-580851-9951224- 12961314-16631930- 19752724-29052968- 30983283-33285121- 52305331-5689 HJACG30 260 895505 AC018512 1957 1-776 HJACG30 260 895505 AC022305 1958 1-878 HJACG30 260 895505 AC002518 1959 1-150 HKACM93 277 1352383 AL158848 1960 1-4314227-44186907- 702812393- 1278813026- 1317114505- 1463414659- 1470115118- 1540516371- 1656817704- 1788818408- 1858018868- 1902119843- 2002321731- 2191123724-25211 HKACM93 277 1352383 AL158848 1961 1-28332990- 34083932-59585960- 60456428-6501 HKGAT94 283 762811 AC025388 1962 1-10401047- 23562415-3968 HKGAT94 283 762811 AL109945 1963 1-10401047- 23562415-3968 HKGAT94 283 762811 AC022307 1964 1-10401047- 23562415-3968 HKGAT94 283 762811 AC025388 1965 1-506 HKGAT94 283 762811 AL109945 1966 1-506 HKGAT94 283 762811 AL109945 1967 1-456 HKGAT94 283 762811 AC022307 1968 1-479 HKGAT94 283 762811 AC022307 1969 1-506 HLHFR58 305 919888 AC020749 1970 1-1006 HLHFR58 305 919888 AC020749 1971 1-336 HNGBC07 372 1037631 AL022339 1972 1-1583 HNGIH43 380 410179 AC018980 1973 1-833147-40454401- 4443 HNGIH43 380 410179 AC018977 1974 1-604 HNGIH43 380 410179 AL356243 1975 1-833146-40444400- 4442 HNGIH43 380 410179 AC018980 1976 1-872 HNTSY18 409 1041383 AC004877 1977 1-175342-474573- 18832536-26322831- 28942999-32315032- 51646664-68207288- 7881 HNTSY18 409 1041383 AC004877 1978 1-421197-13331575- 16981936-19842246- 2304 HOEDE28 424 1036480 AC058820 1979 1-150412-5801115- 17241821-24612640- 4410 HOEDE28 424 1036480 AC058820 1980 1-533676-947959- 1251 HOHBY44 441 873264 AC074201 1981 1-52805527- 59897392-7421 HOHBY44 441 873264 AC074201 1982 1-298 HPDWP28 454 1094609 AP000067 1983 1-818981-13371583- 18232236-2371 HPDWP28 454 1094609 AP000067 1984 1-129 HPICB53 461 1042309 AC002351 1985 1-82959-2236 HPICB53 461 1042309 AC020997 1986 1-1329 HPICB53 461 1042309 AC002351 1987 1-115 HPICB53 461 1042309 AC020997 1988 1-2011064-11261665- 21532308-3502 HPJBK12 462 1011467 AC022033 1989 1-2649 HPJBK12 462 1011467 AC013541 1990 1-2649 HPJBK12 462 1011467 AC022033 1991 1-190 HPJBK12 462 1011467 AC013541 1992 1-190 HPJCL22 463 1146674 AC037447 1993 1-102373-826995- 13151450-15672189- 25152599-27783138- 41324537-46814864- 49985144-53245394- 62116816-69417472- 76477791-88859056- 93689506-97339799- 1010010277- 1098811213- 1175111783- 1183811875- 1247412592-13077 HPJCL22 463 1146674 AC022400 1994 1-102373-826995- 13151450-15672189- 25152599-27783138- 41324537-46814864- 49985144-53245394- 62116816-69417472- 76477791-88859056- 93689506-97339799- 1010010277- 1098811213- 1175111783- 1183711874- 1247312591-13076 HPJCL22 463 1146674 AC037447 1995 1-207 HPJCL22 463 1146674 AC037447 1996 1-2124 HPJCL22 463 1146674 AC022400 1997 1-207 HPJCL22 463 1146674 AC022400 1998 1-21242470- 25672865-2971 HPJEX20 465 1352420 AL080251 1999 1-1821 HPJEX20 465 1352420 AL139283 2000 1-1821 HPJEX20 465 1352420 AL080251 2001 1-313 HPJEX20 465 1352420 AL139283 2002 1-313 HPWAY46 475 1001560 AC019036 2003 1-1399 HPWAY46 475 1001560 AC067828 2004 1-1399 HPWAY46 475 1001560 AC019036 2005 1-788 HPWAY46 475 1001560 AC067828 2006 1-788 HSAUK57 487 772554 AC008860 2007 1-1344 HSAUK57 487 772554 AC025444 2008 1-1344 HSAUK57 487 772554 AC008860 2009 1-340 HSAUK57 487 772554 AC025444 2010 1-340 HSAWD74 491 460527 AC004951 2011 1-16511740-2593 HSAWD74 491 460527 AC004951 2012 1-149 HSAWD74 491 460527 AC004951 2013 1-50575082- 83538404-8996 HSDJL42 503 1036471 AC008676 2014 1-56571-2959 HSLJG37 519 1016920 AC022608 2015 1-2406 HSLJG37 519 1016920 AC022608 2016 1-53430-718 HSLJG37 519 1016920 AC022608 2017 1-351 HSODE04 520 906081 Z99289 2018 1-1365 HSXEQ06 535 1016924 AL390254 2019 1-1593226-45945783- 72547340-77208172- 13712 HSXEQ06 535 1016924 AL356017 2020 1-73505-6801625- 24035814-59729035- 1040311592- 1306313149- 1352913981-19521 HSXEQ06 535 1016924 AL390254 2021 1-126 HSXEQ06 535 1016924 AL356017 2022 1-126 HSXEQ06 535 1016924 AL356017 2023 1-42674-8283271- 34064251-43265040- 51807884-82308404- 86218735-889210277- 10417 HSYAZ50 539 1027673 AC007378 2024 1-2471 HSYAZ50 539 1027673 AC073041 2025 1-2471 HSYAZ50 539 1027673 AC007378 2026 1-467 HSYAZ50 539 1027673 AC073041 2027 1-467 HTHBG43 565 919911 AL139257 2028 1-36130-201330- 7531823-22142331- 24402728-28342920- 30283370-35144153- 52365877-67446813- 71248441-92809527- 995310394- 1053610945- 1136211763- 1184312653- 1295313970- 1418314223- 1472615929- 1629916328- 1675117791- 1809318095- 1871218754- 2462824879-25426 HTHBG43 565 919911 AL139257 2029 1-286 HTHCA18 566 908144 AP002439 2030 1-1800 HTHCA18 566 908144 AP002505 2031 1-1776 HTHCA18 566 908144 AP002439 2032 1-110 HTHCA18 566 908144 AP002505 2033 1-110 HTJML75 570 1040047 AC025036 2034 1-148 HTJML75 570 1040047 AC022232 2035 1-152 HTJML75 570 1040047 AC022231 2036 1-151 HTJML75 570 1040047 AC010694 2037 1-202 HTJML75 570 1040047 AC027300 2038 1-158 HTJML75 570 1040047 AC011953 2039 1-126 HTJML75 570 1040047 AC010694 2040 1-77 HTLIV19 579 1046341 AC055750 2041 1-964 HTLIV19 579 1046341 AC027463 2042 1-964 HTLIV19 579 1046341 AC055750 2043 1-236 HTLIV19 579 1046341 AC027463 2044 1-236 HTOIZ02 588 826312 AC023146 2045 1-21013106-3722 HTOIZ02 588 826312 AC023146 2046 1-278 HVARW53 609 1194812 AC011298 2047 1-6481184-30223943- 40475961-6504 HVARW53 609 1194812 AC011298 2048 1-397

Tables 1D: The polynucleotides or polypeptides, or agonists or antagonists of the present invention can be used in assays to test for one or more biological activities. If these polynucleotides and polypeptides do exhibit activity in a particular assay, it is likely that these molecules may be involved in the diseases associated with the biological activity. Thus, the polynucleotides or polypeptides, or agonists or antagonists could be used to treat the associated disease.

The present invention encompasses methods of detecting, preventing, diagnosing, prognosticating, treating, and/or ameliorating a disease or disorder. In preferred embodiments, the present invention encompasses a method of treating cancer and other hyperproliferative disorders comprising administering to a patient in which such detection, treatment, prevention, and/or amelioration is desired a protein, nucleic acid, or antibody of the invention (or fragment or variant thereof) in an amount effective to detect, prevent, diagnose, prognosticate, treat, and/or ameliorate the cancer and other hyperproliferative disorders.

In another embodiment, the present invention also encompasses methods of detecting, preventing, diagnosing, prognosticating, treating, and/or ameliorating cancer and other hyperproliferative disorders; comprising administering to a patient combinations of the proteins, nucleic acids, or antibodies of the invention (or fragments or variants thereof), sharing similar indications as shown in the corresponding rows in Column 3 of Table 1D.

Table 1D provides information related to biological activities for polynucleotides and polypeptides of the invention (including antibodies, agonists, and/or antagonists thereof). Table 1D also provides information related to assays which may be used to test polynucleotides and polypeptides of the invention (including antibodies, agonists, and/or antagonists thereof) for the corresponding biological activities. The first column (“Gene No.”) provides the gene number in the application for each clone identifier. The second column (“cDNA Clone ID:”) provides the unique clone identifier for each clone as previously described and indicated in Table 1A through Table 1D. The third column (“AA SEQ ID NO:Y”) indicates the Sequence Listing SEQ ID Number for polypeptide sequences encoded by the corresponding cDNA clones (also as indicated in Tables 1A, Table 1B, and Table 2). The fourth column (“Biological Activity”) indicates a biological activity corresponding to the indicated polypeptides (or polynucleotides encoding said polypeptides). The fifth column (“Exemplary Activity Assay”) further describes the corresponding biological activity and also provides information pertaining to the various types of assays which may be performed to test, demonstrate, or quantify the corresponding biological activity.

Table 1D describes the use of, inter alia, FMAT technology for testing or demonstrating various biological activities. Fluorometric microvolume assay technology (FMAT) is a fluorescence-based system which provides a means to perform nonradioactive cell- and bead-based assays to detect activation of cell signal transduction pathways. This technology was designed specifically for ligand binding and immunological assays. Using this technology, fluorescent cells or beads at the bottom of the well are detected as localized areas of concentrated fluorescence using a data processing system. Unbound fluorophore comprising the background signal is ignored, allowing for a wide variety of homogeneous assays. FMAT technology may be used for peptide ligand binding assays, immunofluorescence, apoptosis, cytotoxicity, and bead-based immunocapture assays. See, Miraglia S et. al., “Homogeneous cell and bead based assays for highthroughput screening using fluorometric microvolume assay technology,” Journal of Biomolecular Screening; 4:193-204 (1999). In particular, FMAT technology may be used to test, confirm, and/or identify the ability of polypeptides (including polypeptide fragments and variants) to activate signal transduction pathways. For example, FMAT technology may be used to test, confirm, and/or identify the ability of polypeptides to upregulate production of immunomodulatory proteins (such as, for example, interleukins, GM-CSF, Rantes, and Tumor Necrosis factors, as well as other cellular regulators (e.g. insulin)).

Table 1D also describes the use of kinase assays for testing, demonstrating, or quantifying biological activity. In this regard, the phosphorylation and de-phosphorylation of specific amino acid residues (e.g. Tyrosine, Serine, Threonine) on cell-signal transduction proteins provides a fast, reversible means for activation and de-activation of cellular signal transduction pathways. Moreover, cell signal transduction via phosphorylation/de-phosphorylation is crucial to the regulation of a wide variety of cellular processes (e.g. proliferation, differentiation, migration, apoptosis, etc.). Accordingly, kinase assays provide a powerful tool useful for testing, confirming, and/or identifying polypeptides (including polypeptide fragments and variants) that mediate cell signal transduction events via protein phosphorylation. See e.g., Forrer, P., Tamaskovic R., and Jaussi, R. “Enzyme-Linked Immunosorbent Assay for Measurement of JNK, ERK, and p38 Kinase Activities” Biol. Chem. 379(8-9): 1101-1110 (1998). LENGTHY TABLE REFERENCED HERE US20080103090A1-20080501-T00003 Please refer to the end of the specification for access instructions. Table 1E

Polynucleotides encoding polypeptides of the present invention can be used in assays to test for one or more biological activities. One such biological activity which may be tested includes the ability of polynucleotides and polypeptides of the invention to stimulate up-regulation or down-regulation of expression of particular genes and proteins. Hence, if polynucleotides and polypeptides of the present invention exhibit activity in altering particular gene and protein expression patterns, it is likely that these polynucleotides and polypeptides of the present invention may be involved in, or capable of effecting changes in, diseases associated with the altered gene and protein expression profiles. Hence, polynucleotides, polypeptides, or antibodies of the present invention could be used to treat said associated diseases.

TaqMan® assays may be performed to assess the ability of polynucleotides (and polypeptides they encode) to alter the expression pattern of particular “target” genes. TaqMan® reactions are performed to evaluate the ability of a test agent to induce or repress expression of specific genes in different cell types. TaqMan® gene expression quantification assays (“TaqMan® assays”) are well known to, and routinely performed by, those of ordinary skill in the art. TaqMan® assays are performed in a two step reverse transcription/polymerase chain reaction (RT-PCR). In the first (RT) step, cDNA is reverse transcribed from total RNA samples using random hexamer primers. In the second (PCR) step, PCR products are synthesized from the cDNA using gene specific primers.

To quantify gene expression the Taqman® PCR reaction exploits the 5′ nuclease activity of AmpliTaq Gold® DNA Polymerase to cleave a Taqman® probe (distinct from the primers) during PCR. The Taqman® probe contains a reporter dye at the 5′-end of the probe and a quencher dye at the 3′ end of the probe. When the probe is intact, the proximity of the reporter dye to the quencher dye results in suppression of the reporter fluorescence. During PCR, if the target of interest is present, the probe specifically anneals between the forward and reverse primer sites. AmpliTaq Fold DNA Polymerase then cleaves the probe between the reporter and quencher when the probe hybridizes to the target, resulting in increased fluorescence of the reporter (see FIG. 2). Accumulation of PCR products is detected directly by monitoring the increase in fluorescence of the reporter dye.

After the probe fragments are displaced from the target, polymerization of the strand continues. The 3′-end of the probe is blocked to prevent extension of the probe during PCR. This process occurs in every cycle and does not interfere with the exponential accumulation of product. The increase in fluorescence signal is detected only if the target sequence is complementary to the probe and is amplified during PCR. Because of these requirements, any nonspecific amplification is not detected.

For test sample preparation, vector controls or constructs containing the coding sequence for the gene of interest are transfected into cells, such as for example 293T cells, and supernatants collected after 48 hours. For cell treatment and RNA isolation, multiple primary human cells or human cell lines are used; such cells may include but are not limited to, Normal Human Dermal Fibroblasts, Aortic Smooth Muscle, Human Umbilical Vein Endothelial Cells, HepG2, Daudi, Jurkat, U937, Caco, and THP-1 cell lines. Cells are plated in growth media and growth is arrested by culturing without media change for 3 days, or by switching cells to low serum media and incubating overnight. Cells are treated for 1, 6, or 24 hours with either vector control supernatant or sample supernatant (or purified/partially purified protein preparations in buffer). Total RNA is isolated; for example, by using TRIZOL™ extraction or by using the Ambion RNAqueous™-4PCR RNA isolation system. Expression levels of multiple genes are analyzed using TAQMAN, and expression in the test sample is compared to control vector samples to identify genes induced or repressed. Each of the above described techniques are well known to, and routinely performed by, those of ordinary skill in the art.

Table 1E indicates particular disease classes and preferred indications for which polynucleotides, polypeptides, or antibodies of the present invention may be used in detecting, diagnosing, preventing, treating and/or ameliorating said diseases and disorders based on “target” gene expression patterns which may be up- or down-regulated by polynucleotides (and the encoded polypeptides) corresponding to each indicated cDNA Clone ID (shown in Table 1E, Column 2).

Thus, in preferred embodiments, the present invention encompasses a method of detecting, diagnosing, preventing, treating, and/or ameliorating a disease or disorder listed in the “Disease Class” and/or “Preferred Indication” columns of Table 1E; comprising administering to a patient in which such detection, diagnosis, prevention, or treatment is desired a protein, nucleic acid, or antibody of the invention (or fragment or variant thereof) in an amount effective to detect, diagnose, prevent, treat, or ameliorate the disease or disorder. The first and second columns of Table 1D show the “Gene No.” and “cDNA Clone ID No.”, respectively, indicating certain nucleic acids and proteins (or antibodies against the same) of the invention (including polynucleotide, polypeptide, and antibody fragments or variants thereof) that may be used in detecting, diagnosing, preventing, treating, or ameliorating the disease(s) or disorder(s) indicated in the corresponding row in the “Disease Class” or “Preferred Indication” Columns of Table 1E.

In another embodiment, the present invention also encompasses methods of detecting, diagnosing, preventing, treating, or ameliorating a disease or disorder listed in the “Disease Class” or “Preferred Indication” Columns of Table 1E; comprising administering to a patient combinations of the proteins, nucleic acids, or antibodies of the invention (or fragments or variants thereof), sharing similar indications as shown in the corresponding rows in the “Disease Class” or “Preferred Indication” Columns of Table 1E.

The “Disease Class” Column of Table 1E provides a categorized descriptive heading for diseases, disorders, and/or conditions (more fully described below) that may be detected, diagnosed, prevented, treated, or ameliorated by a protein, nucleic acid, or antibody of the invention (or fragment or variant thereof).

The “Preferred Indication” Column of Table 1E describes diseases, disorders, and/or conditions that may be detected, diagnosed, prevented, treated, or ameliorated by a protein, nucleic acid, or antibody of the invention (or fragment or variant thereof).

The “Cell Line” and “Exemplary Targets” Columns of Table 1E indicate particular cell lines and target genes, respectively, which may show altered gene expression patterns (i.e., up- or down-regulation of the indicated target gene) in Taqman assays, performed as described above, utilizing polynucleotides of the cDNA Clone ID shown in the corresponding row. Alteration of expression patterns of the indicated “Exemplary Target” genes is correlated with a particular “Disease Class” and/or “Preferred Indication” as shown in the corresponding row under the respective column headings.

The “Exemplary Accessions” Column indicates GenBank Accessions (available online through the National Center for Biotechnology Information (CBI) at www.ncbi.nlm.nih.gov/) which correspond to the “Exemplary Targets” shown in the adjacent row.

The recitation of “Cancer” in the “Disease Class” Column indicates that the corresponding nucleic acid and protein, or antibody against the same, of the invention (or fragment or variant thereof) may be used for example, to detect, diagnose, prevent, treat, and/or ameliorate neoplastic diseases and/or disorders (e.g., leukemias, cancers, etc., as described below under “Hyperproliferative Disorders”).

The recitation of “Immune” in the “Disease Class” column indicates that the corresponding nucleic acid and protein, or antibody against the same, of the invention (or fragment or variant thereof), may be used for example, to detect, diagnose, prevent, treat, and/or ameliorate diseases and/or disorders relating to neoplastic diseases (e.g., as described below under “Hyperproliferative Disorders”), blood disorders (e.g., as described below under “Immune Activity” “Cardiovascular Disorders” and/or “Blood-Related Disorders”), and infections (e.g., as described below under “Infectious Disease”).

The recitation of “Angiogenesis” in the “Disease Class” column indicates that the corresponding nucleic acid and protein, or antibody against the same, of the invention (or fragment or variant thereof), may be used for example, to detect, diagnose, treat, prevent, and/or ameliorate diseases and/or disorders relating to neoplastic diseases (e.g., as described below under “Hyperproliferative Disorders”), diseases and/or disorders of the cardiovascular system (e.g., as described below under “Cardiovascular Disorders”), diseases and/or disorders involving cellular and genetic abnormalities (e.g., as described below under “Diseases at the Cellular Level”), diseases and/or disorders involving angiogenesis (e.g., as described below under “Anti-Angiogenesis Activity”), to promote or inhibit cell or tissue regeneration (e.g., as described below under “Regeneration”), or to promote wound healing (e.g., as described below under “Wound Healing and Epithelial Cell Proliferation”).

The recitation of “Diabetes” in the “Disease Class” column indicates that the corresponding nucleic acid and protein, or antibody against the same, of the invention (or fragment or variant thereof), may be used for example, to detect, diagnose, treat, prevent, and/or ameliorate diabetes (including diabetes mellitus types I and II), as well as diseases and/or disorders associated with, or consequential to, diabetes (e.g. as described below under “Endocrine Disorders,” “Renal Disorders,” and “Gastrointestinal Disorders”). TABLE 1E Gene cDNA Clone Disease Exemplary Exemplary No. ID Class Preferred Indications Cell Line Targets Accessions 13 HAGDG59 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, AOSMC Vegf1 gb|AF024710|AF024710 and/or amelioration of diseases and disorders involving angiogenesis, wound healing, neoplasia (particularly including, but not limited to, tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(AOSMC cells are aortic smooth muscle cells). 13 HAGDG59 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, HEK293 TSP-1 gb|X04665|HSTHROMR and/or amelioration of diseases and disorders involving angiogenesis, wound healing, neoplasia (particularly including, but not limited to, tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(The HEK293 cell line is a human embryonal kidney epithelial cell line available through the ATCC ™ as cell line number CRL-1573). 13 HAGDG59 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, HUVEC Vegf1 gb|AF024710|AF024710 and/or amelioration of diseases and disorders involving angiogenesis, wound healing, neoplasia (particularly including, but not limited to, tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(HUVEC cells are human umbilical vein endothelial cells). 13 HAGDG59 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, SK-N-MC neuroblastoma CyclooxVegf1 gb|AF024710|AF024710 and/or amelioration of diseases and disorders involving angiogenesis, wound healing, neoplasia (particularly including, but not limited to, tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(The SK-N-MC neuroblastoma cell line is a cell line derived from human brain tissue available through the ATCC ™ as cell line number HTB- 10). 13 HAGDG59 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) Caco-2 M1 RIBO gb|X59543|HSRIREM1gb|X60011|HSP53002gb| such as described herein under the heading “Hyperproliferative Rp53TAA6 I34297|I34297 Disorders$$ (particularly including, but not limited to, cancer involving cells of the gastrointestinal tract). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving the gastrointestinal tract. (The Caco-2 cell line is a human colorectal adenocarcinoma cell line available through the ATCC ™ as cell line number HTB-37). 13 HAGDG59 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) HUVEC bcl-2Cyclin D gb|X06487|HSBCL2IGgb|BC000076|BC000076 such as described herein under the heading “Hyperproliferative Disordersî (particularly including, but not limited to, cancers involving endothelial cells). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving endothelial cells. (HUVEC cells are human umbilical vein endothelial cells). 13 HAGDG59 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) SK-N- Baxbcl- gb|AF250190|AF250190gb| such as described herein under the heading “Hyperproliferative MC 2Cyclin D X06487| Disordersî (particularly including, but not limited to cancers involving neuroblastoma HSBCL2IGgb| cells of the brain/central nervous system (e.g. neural epithelium)). BC000076|BC000076 Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving the brain or central nervous system. (The SK-N-MC neuroblastoma cell line is a cell line derived from human brain tissue available through the ATCC ™ as cell line number HTB-10). 13 HAGDG59 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) U937 beta- gb|AR034832|AR034832gb|V00507|HSDHFRgb| such as described herein under the heading “Hyperproliferative cateninCyclin X59543|HSRIREM1 Disordersî (particularly including, but not limited to, cancers of immune D3DHFR cells, such as monocytes). Highly preferred embodiments of the M1 RIBO R invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving cells of the immune system (such as monocytes). (The U-937 cell line is a human monocyte cell line available through the ATCC ™ as cell line number CRL-1593.2) 13 HAGDG59 Immune Highly preferred indications include immunological disorders such as AOSMC CIS3GAT gb|AB006967|AB006967gb| described herein under the heading “Immune Activity” and/or “Blood- A1IL1B X17254| Related Disorders” (particularly including, but not limited to, immune HSERYF1gb| disorders involving muscle tissues and the cardiovascular system (e.g. X02532|HSIL1BR heart, lungs, circulatory system)). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving muscle tissue or the cardiovascular system). (AOSMC cells are human aortic smooth muscle cells). 13 HAGDG59 Immune Highly preferred indications include immunological disorders such as Caco-2 TNF gb|AJ270944|HSA27094 described herein under the heading “Immune Activity” and/or “Blood- Related Disorders” (particularly including, but not limited to, immune disorders involving the cells of the gastrointestinal tract). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving cells of the gastrointestinal tract). (The Caco-2 cell line is a human colorectal adenocarcinoma cell line available through the ATCC ™ as cell line number HTB-37). 13 HAGDG59 Immune Highly preferred indications include immunological disorders such as HEK293 GATA3 gb|X55037|HSGATA3 described herein under the heading “Immune Activity” and/or “Blood- Related Disorders” (particularly including, but not limited to, immune disorders involving epithelial cells or the renal system). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving epithelial cells or the renal system). (The 293 cell line is a human embryonal kidney epithelial cell line available through the ATCC ™ as cell line number CRL-1573). 13 HAGDG59 Immune Highly preferred indications include immunological disorders such as HUVEC CD30HLA- gb|X12705|HSBCDFIAgb| described herein under the heading “Immune Activity” and/or “Blood- cIL5TNF AJ270944| Related Disorders” (particularly including, but not limited to, immune HSA27094 disorders involving endothelial cells). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving endothelial cells). (HUVEC cells are human umbilical vein endothelial cells). 13 HAGDG59 Immune Highly preferred indications include immunological disorders such as Jurkat Rag1TNF gb|M29474|HUMRAG1gb| described herein under the heading “Immune Activity” and/or “Blood- AJ270944| Related Disorders” (particularly including, but not limited to, immune HSA27094 disorders involving T-cells). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving T-cells). (The Jurkat cell line is a human T lymphocyte cell line available through the ATCC ™ as cell line number TIB-152). 13 HAGDG59 Immune Highly preferred indications include immunological disorders such as Liver LTBR gb|AK027080|AK027080 described herein under the heading “Immune Activity” and/or “Blood- Related Disorders” (particularly including, but not limited to, immune disorders involving cells of the hepatic system). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving cells of the hepatic system). 13 HAGDG59 Immune Highly preferred indications include immunological disorders such as SK-N- CIS3GAT gb|AB006967|AB006967gb| described herein under the heading “Immune Activity” and/or “Blood- MC A1HLA-c X17254| Related Disorders” (particularly including, but not limited to, immune neuroblastoma HSERYF1 disorders involving the central nervous system). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving the central nervous sytem). (The SK-N-MC neuroblastoma cell line is a cell line derived from human brain tissue and is available through the ATCC ™ as cell line number HTB-10). 13 HAGDG59 Immune Highly preferred indications include immunological disorders such as T-cell- CD40Granzyme B gb|AJ300189|HSA30018gb| described herein under the heading “Immune Activity” and/or “Blood- Mar. 31, 2000 J04071| Related Disorders” (particularly including, but not limited to, immune HUMCSE disorders involving T-cells). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving T-cells). 13 HAGDG59 Immune Highly preferred indications include immunological disorders such as U937 CD69TNF gb|Z22576|HSCD69GNAgb| described herein under the heading “Immune Activity” and/or “Blood- AJ270944| Related Disorders” (particularly including, but not limited to, immune HSA27094 disorders involving monocytes). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving monocytes). (The U937 cell line is a human monocyte cell line available through the ATCC ™ as cell line number CRL-1593.2). 79 HCHNF25 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, Caco-2 ICAMVCAM gb|X06990|HSICAM1gb| and/or amelioration of diseases and disorders involving angiogenesis, A30922| wound healing, neoplasia (particularly including, but not limited to, A30922 tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(The Caco-2 cell line is a human colorectal adenocarcinoma cell line available through the ATCC ™ as cell line number HTB-37). 79 HCHNF25 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, Daudi Vegf1 gb|AF024710|AF024710 and/or amelioration of diseases and disorders involving angiogenesis, wound healing, neoplasia (particularly including, but not limited to, tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(The Daudi cell line is a human B lymphoblast cell line available through the ATCC ™ as cell line number CCL-213). 79 HCHNF25 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, HUVEC Vegf1 gb|AF024710|AF024710 and/or amelioration of diseases and disorders involving angiogenesis, wound healing, neoplasia (particularly including, but not limited to, tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(HUVEC cells are human umbilical vein endothelial cells). 79 HCHNF25 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, Jurkat VCAM gb|A30922|A30922 and/or amelioration of diseases and disorders involving angiogenesis, wound healing, neoplasia (particularly including, but not limited to, tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(The Jurkat cell line is a human T lymphocyte cell line available through the ATCC ™ as cell line number TIB-152). 79 HCHNF25 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, NHDF PAI gb|X12701|HSENDPAI and/or amelioration of diseases and disorders involving angiogenesis, wound healing, neoplasia (particularly including, but not limited to, tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(NHDF cells are normal human dermal fibroblasts). 79 HCHNF25 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, THP1 Vegf1 gb|AF024710|AF024710 and/or amelioration of diseases and disorders involving angiogenesis, wound healing, neoplasia (particularly including, but not limited to, tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(The THP-1 cell line is a human monocyte cell line available through the ATCC ™ as cell line number TIB-202). 79 HCHNF25 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, U937 VCAM gb|A30922|A30922 and/or amelioration of diseases and disorders involving angiogenesis, wound healing, neoplasia (particularly including, but not limited to, tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(The U937 cell line is a human monocyte cell line available through the ATCC ™ as cell line number CRL-1593.2). 79 HCHNF25 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) AOSMC Cyclin D2 gb|X68452|HSCYCD2 such as described herein under the heading “Hyperproliferative Disordersî (particularly including, but not limited to, cancers of muscle tissues and the cardiovascular system (e.g. heart, lungs, circulatory system)). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders. (AOSMC cells are aortic smooth muscle cells). 79 HCHNF25 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) Caco-2 c- gb|BC004490|BC004490 such as described herein under the heading “Hyperproliferative fosU66469 Disordersî (particularly including, but not limited to, cancer involving p53 cells of the gastrointestinal tract). Highly preferred embodiments of the regulated invention include methods of preventing, detecting, diagnosing, treating gene and/or ameliorating cancer and hyperproliferative disorders involving the gastrointestinal tract. (The Caco-2 cell line is a human colorectal adenocarcinoma cell line available through the ATCC ™ as cell line number HTB-37). 79 HCHNF25 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) Daudi Cyclin A1 gb|U97680|HSU97680 such as described herein under the heading “Hyperproliferative Disordersî (particularly including, but not limited to, cancers of immune cells, such as B-cells). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving immune cells (such as B-cells). (The Daudi cell line is a human B lymphoblast cell line available through the ATCC ™ as cell line number CCL-213). 79 HCHNF25 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) HUVEC Cyclin gb|U97680|HSU97680gb| such as described herein under the heading “Hyperproliferative A1Cyclin BC000076| Disordersî (particularly including, but not limited to, cancers involving DCyclin BC000076gb| endothelial cells). Highly preferred embodiments of the invention D2 X68452|HSCYCD2 include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving endothelial cells. (HUVEC cells are human umbilical vein endothelial cells). 79 HCHNF25 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) Jurkat DHFRp21 gb|V00507|HSDHFRgb| such as described herein under the heading “Hyperproliferative U66469 BC000275| Disordersî (particularly including, but not limited to, cancers of immune p53 BC000275 cells, such as T-cells). Highly preferred embodiments of the invention regulated include methods of preventing, detecting, diagnosing, treating and/or gene ameliorating cancer and hyperproliferative disorders involving immune cells (such as T-cells). (The Jurkat cell line is a human T lymphocyte cell line available through the ATCC ™ as cell line number TIB-152). 79 HCHNF25 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) Liver p21 gb|BC000275|BC000275 such as described herein under the heading “Hyperproliferative Disordersî (particularly including, but not limited to, cancers involving cells of the hepatic system). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving cells of the hepatic system. 79 HCHNF25 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) THP1 c-fos gb|BC004490|BC004490 such as described herein under the heading “Hyperproliferative Disordersî (particularly including, but not limited to, cancers of immune cells, such as monocytes). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving cells of the immune system (such as monocytes). (The THP-1 cell line is a human monocyte cell line available through the ATCC ™ as cell line number TIB-202). 79 HCHNF25 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) U937 Cyclin gb|U97680|HSU97680gb| such as described herein under the heading “Hyperproliferative A1Cyclin BC000076| Disordersî (particularly including, but not limited to, cancers of immune DCyclin BC000076gb| cells, such as monocytes). Highly preferred embodiments of the D2 X68452|HSCYCD2 invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving cells of the immune system (such as monocytes). (The U-937 cell line is a human monocyte cell line available through the ATCC ™ as cell line number CRL-1593.2) 79 HCHNF25 Immune Highly preferred indications include immunological disorders such as Caco-2 CCR4CIS3 gb|AB023888|AB023888gb| described herein under the heading “Immune Activity” and/or “Blood- ICAMVCAM AB006967| Related Disorders” (particularly including, but not limited to, immune AB006967gb| disorders involving the cells of the gastrointestinal tract). Highly X06990|HSICAM1gb| preferred embodiments of the invention include methods of preventing, A30922| detecting, diagnosing, treating and/or ameliorating disorders of the A30922 immune system (particularly including, but not limited to, immune disorders involving cells of the gastrointestinal tract). (The Caco-2 cell line is a human colorectal adenocarcinoma cell line available through the ATCC ™ as cell line number HTB-37). 79 HCHNF25 Immune Highly preferred indications include immunological disorders such as Daudi Rag1Rag2 gb|M29474|HUMRAG1gb| described herein under the heading “Immune Activity” and/or “Blood- AY011962| Related Disorders” (particularly including, but not limited to, immune AY011962 disorders involving the B-cells). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving B-cells). (The Daudi cell line is a human B lymphoblast cell line available through the ATCC ™ as cell line number CCL-213). 79 HCHNF25 Immune Highly preferred indications include immunological disorders such as HUVEC CD25TNF gb|X03137|HSIL2RG7gb| described herein under the heading “Immune Activity” and/or “Blood- AJ270944| Related Disorders” (particularly including, but not limited to, immune HSA27094 disorders involving endothelial cells). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving endothelial cells). (HUVEC cells are human umbilical vein endothelial cells). 79 HCHNF25 Immune Highly preferred indications include immunological disorders such as Jurkat CD28IL2V gb|AF222342|AF222342gb| described herein under the heading “Immune Activity” and/or “Blood- CAM X61155| Related Disorders” (particularly including, but not limited to, immune HSARTIL2gb| disorders involving T-cells). Highly preferred embodiments of the A30922|A30922 invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving T-cells). (The Jurkat cell line is a human T lymphocyte cell line available through the ATCC ™ as cell line number TIB-152). 79 HCHNF25 Immune Highly preferred indications include immunological disorders such as Liver CCR4CD2 gb|AB023888|AB023888gb| described herein under the heading “Immune Activity” and/or “Blood- 8CXCR3R AF222342| Related Disorders” (particularly including, but not limited to, immune ag2 AF222342gb| disorders involving cells of the hepatic system). Highly preferred Z79783|HSCKRL2gb| embodiments of the invention include methods of preventing, detecting, AY011962| diagnosing, treating and/or ameliorating disorders of the immune AY011962 system (particularly including, but not limited to, immune disorders involving cells of the hepatic system). 79 HCHNF25 Immune Highly preferred indications include immunological disorders such as NHDF CIS3Rag1 gb|AB006967|AB006967gb| described herein under the heading “Immune Activity” and/or “Blood- M29474| Related Disorders” (particularly including, but not limited to, immune HUMRAG1 disorders involving the skin). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving the skin). (NHDF cells are normal human dermal fibroblasts). 79 HCHNF25 Immune Highly preferred indications include immunological disorders such as THP1 CD28CIS3 gb|AF222342|AF222342gb| described herein under the heading “Immune Activity” and/or “Blood- CXCR3 AB006967| Related Disorders” (particularly including, but not limited to, immune AB006967gb| disorders involving monocytes). Highly preferred embodiments of the Z79783|HSCKRL2 invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving monocytes). (The THP1 cell line is a human monocyte cell line available through the ATCC ™ as cell line number TIB-202). 79 HCHNF25 Immune Highly preferred indications include immunological disorders such as U937 TNFVCAM gb|AJ270944|HSA27094gb| described herein under the heading “Immune Activity” and/or “Blood- A30922| Related Disorders” (particularly including, but not limited to, immune A30922 disorders involving monocytes). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving monocytes). (The U937 cell line is a human monocyte cell line available through the ATCC ™ as cell line number CRL-1593.2). 105 HDPBQ71 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, AOSMC Flt1VCAM gb|AF063657|AF063657gb| and/or amelioration of diseases and disorders involving angiogenesis, A30922| wound healing, neoplasia (particularly including, but not limited to, A30922 tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(AOSMC cells are aortic smooth muscle cells). 105 HDPBQ71 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, Caco-2 Vegf1 gb|AF024710|AF024710 and/or amelioration of diseases and disorders involving angiogenesis, wound healing, neoplasia (particularly including, but not limited to, tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(The Caco-2 cell line is a human colorectal adenocarcinoma cell line available through the ATCC ™ as cell line number HTB-37). 105 HDPBQ71 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, Daudi ICAM gb|X06990|HSICAM1 and/or amelioration of diseases and disorders involving angiogenesis, wound healing, neoplasia (particularly including, but not limited to, tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(The Daudi cell line is a human B lymphoblast cell line available through the ATCC ™ as cell line number CCL-213). 105 HDPBQ71 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, HEK293 CyclooxFlt gb|AF063657|AF063657gb| and/or amelioration of diseases and disorders involving angiogenesis, 1iNOS X85761| wound healing, neoplasia (particularly including, but not limited to, HSNOS2E3 tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(The HEK293 cell line is a human embryonal kidney epithelial cell line available through the ATCC ™ as cell line number CRL-1573). 105 HDPBQ71 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, HUVEC Flt1TSP- gb|AF063657|AF063657gb| and/or amelioration of diseases and disorders involving angiogenesis, 1VCAM X04665| wound healing, neoplasia (particularly including, but not limited to, HSTHROMRgb| tumor metastases), and cardiovascular diseases and disorders; as A30922|A30922 described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(HUVEC cells are human umbilical vein endothelial cells). 105 HDPBQ71 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, Jurkat Flt1Vegf1 gb|AF063657|AF063657gb| and/or amelioration of diseases and disorders involving angiogenesis, AF024710| wound healing, neoplasia (particularly including, but not limited to, AF024710 tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(The Jurkat cell line is a human T lymphocyte cell line available through the ATCC ™ as cell line number TIB-152). 105 HDPBQ71 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, Liver VCAM gb|A30922|A30922 and/or amelioration of diseases and disorders involving angiogenesis, wound healing, neoplasia (particularly including, but not limited to, tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.” 105 HDPBQ71 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, NHDF TSP- gb|X04665|HSTHROMRgb| and/or amelioration of diseases and disorders involving angiogenesis, 1Vegf1 AF054710| wound healing, neoplasia (particularly including, but not limited to, AF024710 tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(NHDF cells are normal human dermal fibroblasts). 105 HDPBQ71 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, T cell ICAMVegf1 gb|X06990|HSICAM1gb| and/or amelioration of diseases and disorders involving angiogenesis, AF024710| wound healing, neoplasia (particularly including, but not limited to, AF024710 tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.” 105 HDPBQ71 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, THP1 VCAM gb|A30922|A30922 and/or amelioration of diseases and disorders involving angiogenesis, wound healing, neoplasia (particularly including, but not limited to, tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(The THP-1 cell line is a human monocyte cell line available through the ATCC ™ as cell line number TIB-202). 105 HDPBQ71 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, U937 VCAM gb|A30922|A30922 and/or amelioration of diseases and disorders involving angiogenesis, wound healing, neoplasia (particularly including, but not limited to, tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(The U937 cell line is a human monocyte cell line available through the ATCC ™ as cell line number CRL-1593.2). 105 HDPBQ71 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) Caco-2 p21TAA6 gb|BC000275|BC000275gb| such as described herein under the heading “Hyperproliferative I34297| Disordersî (particularly including, but not limited to, cancer involving I34297 cells of the gastrointestinal tract). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving the gastrointestinal tract. (The Caco-2 cell line is a human colorectal adenocarcinoma cell line available through the ATCC ™ as cell line number HTB-37). 105 HDPBQ71 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) Daudi Cyclin D2 gb|X68452|HSCYCD2 such as described herein under the heading “Hyperproliferative Disordersî (particularly including, but not limited to, cancers of immune cells, such as B-cells). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving immune cells (such as B-cells). (The Daudi cell line is a human B lymphoblast cell line available through the ATCC ™ as cell line number CCL-213). 105 HDPBQ71 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) HEK293 c- gb|BC006175|BC006175gb| such as described herein under the heading “Hyperproliferative junDHFRU V00507| Disordersî (particularly including, but not limited to, cancers of 66469.p53 HSDHFR epithelial cells or cancers involving the renal system). Highly preferred regulated embodiments of the invention include methods of preventing, detecting, gene diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving epithelial cells or the renal system. (The 293 cell line human embryonal kidney epithelial cell line available through the ATCC ™ as cell line number CRL-1573). 105 HDPBQ71 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) HUVEC beta- gb|U97680|HSU97680gb| such as described herein under the heading “Hyperproliferative cateninCyclin X68452| Disordersî (particularly including, but not limited to, cancers involving A1Cyclin HSCYCD2 endothelial cells). Highly preferred embodiments of the invention D2 include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving endothelial cells. (HUVEC cells are human umbilical vein endothelial cells). 105 HDPBQ71 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) Liver Cyclin D3 gb|AR034832|AR034832 such as described herein under the heading “Hyperproliferative Disordersî (particularly including, but not limited to, cancers involving cells of the hepatic system). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving cells of the hepatic system. 105 HDPBQ71 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) NHDF bcl-2beta- gb|X06487|HSBCL2IGgb| such as described herein under the heading “Hyperproliferative cateninCyclin AR034832| Disordersî (particularly including, but not limited to cancers involving D3DHFR AR034832gb| cells of the skin). Highly preferred embodiments of the invention M1 RIBO V00507|HSDHFRgb| include methods of preventing, detecting, diagnosing, treating and/or RU66469 X59543| ameliorating cancer and hyperproliferative disorders involving skin p53 HSRIREM1 cells. (NHDF cells are normal human dermal fibroblasts). regulated gene 105 HDPBQ71 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) T cell Cyclin gb|BC000076|BC000076gb| such as described herein under the heading “Hyperproliferative DDHFRM V00507| Disordersî (particularly including, but not limited to, cancers of immune 1 RIBO HSDHFRgb| cells, such as T-cells). Highly preferred embodiments of the invention Rp21 X59543|HSRIREM1gb| include methods of preventing, detecting, diagnosing, treating and/or BC000275| ameliorating cancer and hyperproliferative disorders involving cells of BC000275 the immune system (such as T-cells). 105 HDPBQ71 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) THP1 Cyclin gb|U97680|HSU97680gb| such as described herein under the heading “Hyperproliferative A1Cyclin X68452| Disordersî (particularly including, but not limited to, cancers of immune D2 HSCYCD2 cells, such as monocytes). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving cells of the immune system (such as monocytes). (The THP-1 cell line is a human monocyte cell line available through the ATCC ™ as cell line number TIB-202). 105 HDPBQ71 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) U937 Cyclin gb|U97680|HSU97680gb| such as described herein under the heading “Hyperproliferative A1Cyclin BC000076| Disordersî (particularly including, but not limited to, cancers of immune Dp21 BC000076gb| cells, such as monocytes). Highly preferred embodiments of the BC000275|BC000275 invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving cells of the immune system (such as monocytes). (The U-937 cell line is a human monocyte cell line available through the ATCC ™ as cell line number CRL-1593.2) 105 HDPBQ71 Immune Highly preferred indications include immunological disorders such as AOSMC IL1BVCAM gb|X02532|HSIL1BRgb| described herein under the heading “Immune Activity” and/or “Blood- A30922| Related Disorders” (particularly including, but not limited to, immune A30922 disorders involving muscle tissues and the cardiovascular system (e.g. heart, lungs, circulatory system)). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving muscle tissue or the cardiovascular system). (AOSMC cells are human aortic smooth muscle cells). 105 HDPBQ71 Immune Highly preferred indications include immunological disorders such as Daudi c- gb|AF055377|AF055377gb| described herein under the heading “Immune Activity” and/or “Blood- mafCD25C X03137| Related Disorders” (particularly including, but not limited to, immune XCR3 Granzyme HSIL2RG7gb| disorders involving the B-cells). Highly preferred embodiments of the BICAM Z79783|HSCKRL2gb| invention include methods of preventing, detecting, diagnosing, treating J04071| and/or ameliorating disorders of the immune system (particularly HUMCSEgb|X06990| including, but not limited to, immune disorders involving B-cells). (The HSICAM1 Daudi cell line is a human B lymphoblast cell line available through the ATCC ™ as cell line number CCL-213). 105 HDPBQ71 Immune Highly preferred indications include immunological disorders such as HEK293 CCR4TNF gb|AB023888|AB023888gb| described herein under the heading “Immune Activity” and/or “Blood- AJ270944| Related Disorders” (particularly including, but not limited to, immune HSA27094 disorders involving epithelial cells or the renal system). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving epithelial cells or the renal system). (The 293 cell line is a human embryonal kidney epithelial cell line available through the ATCC ™ as cell line number CRL-1573). 105 HDPBQ71 Immune Highly preferred indications include immunological disorders such as HUVEC Rag2VCAM gb|AY011962|AY011962gb| described herein under the heading “Immune Activity” and/or “Blood- A30922| Related Disorders” (particularly including, but not limited to, immune A30922 disorders involving endothelial cells). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving endothelial cells). (HUVEC cells are human umbilical vein endothelial cells). 105 HDPBQ71 Immune Highly preferred indications include immunological disorders such as Jurkat c- gb|AF055377|AF055377gb| described herein under the heading “Immune Activity” and/or “Blood- mafCD69TNF Z22576| Related Disorders” (particularly including, but not limited to, immune HSCD69GNAgb| disorders involving T-cells). Highly preferred embodiments of the AJ270944| invention include methods of preventing, detecting, diagnosing, treating HSA27094 and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving T-cells). (The Jurkat cell line is a human T lymphocyte cell line available through the ATCC ™ as cell line number TIB-152). 105 HDPBQ71 Immune Highly preferred indications include immunological disorders such as Liver VCAM gb|A30922|A30922 described herein under the heading “Immune Activity” and/or “Blood- Related Disorders” (particularly including, but not limited to, immune disorders involving cells of the hepatic system). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving cells of the hepatic system). 105 HDPBQ71 Immune Highly preferred indications include immunological disorders such as NHDF HLA- gb|AK027080|AK027080gb| described herein under the heading “Immune Activity” and/or “Blood- cLTBRRag1 M29474| Related Disorders” (particularly including, but not limited to, immune HUMRAG1 disorders involving the skin). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving the skin). (NHDF cells are normal human dermal fibroblasts). 105 HDPBQ71 Immune Highly preferred indications include immunological disorders such as SK-N- CD40TNF gb|AJ300189|HSA30018gb| described herein under the heading “Immune Activity” and/or “Blood- MC AJ270944| Related Disorders” (particularly including, but not limited to, immune neuroblastoma HSA27094 disorders involving the central nervous system). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving the central nervous sytem). (The SK-N-MC neuroblastoma cell line is a cell line derived from human brain tissue and is available through the ATCC ™ as cell line number HTB-10). 105 HDPBQ71 Immune Highly preferred indications include immunological disorders such as T cell CD69CTL gb|Z22576|HSCD69GNAgb| described herein under the heading “Immune Activity” and/or “Blood- A4Granzyme AF316875| Related Disorders” (particularly including, but not limited to, immune BICAMIF AF316875gb| disorders involving T-cells). Highly preferred embodiments of the NgIL5LTB J04071|HUMCSEgb| invention include methods of preventing, detecting, diagnosing, treating RRag2 X06990| and/or ameliorating disorders of the immune system (particularly HSICAM1gb| including, but not limited to, immune disorders involving T-cells). X87308|HSRNAIGgb| X12705| HSBCDFIAgb| AK027080|AK027080gb| AY011962| AY011962 105 HDPBQ71 Immune Highly preferred indications include immunological disorders such as THP1 CCR3CD30 gb|AB023887|AB023887gb| described herein under the heading “Immune Activity” and/or “Blood- Il6Rag2V X04403| Related Disorders” (particularly including, but not limited to, immune CAM HS26KDARgb| disorders involving monocytes). Highly preferred embodiments of the AY011962| invention include methods of preventing, detecting, diagnosing, treating AY011962gb|A30922| and/or ameliorating disorders of the immune system (particularly A30922 including, but not limited to, immune disorders involving monocytes). (The THP1 cell line is a human monocyte cell line available through the ATCC ™ as cell line number TIB-202). 105 HDPBQ71 Immune Highly preferred indications include immunological disorders such as U937 CD69TNF gb|Z22576|HSCD69GNAgb| described herein under the heading “Immune Activity” and/or “Blood- VCAM AJ270944| Related Disorders” (particularly including, but not limited to, immune HSA27094gb| disorders involving monocytes). Highly preferred embodiments of the A30922|A30922 invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving monocytes). (The U937 cell line is a human monocyte cell line available through the ATCC ™ as cell line number CRL-1593.2). 187 HFCCQ50 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, TF-1 TSP-1 gb|X04665|HSTHROMR and/or amelioration of diseases and disorders involving angiogenesis, wound healing, neoplasia (particularly including, but not limited to, tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(The TF-1 cell line is a human erythroblast cell line available through the ATCC ™ as cell line number CRL-2003). 187 HFCCQ50 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, U937 ICAM gb|X06990|HSICAM1 and/or amelioration of diseases and disorders involving angiogenesis, wound healing, neoplasia (particularly including, but not limited to, tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(The U937 cell line is a human monocyte cell line available through the ATCC ™ as cell line number CRL-1593.2). 187 HFCCQ50 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) TF-1 Cyclin gb|X68452|HSCYCD2gb| such as described herein under the heading “Hyperproliferative D2M1 X59543| Disordersî (particularly including, but not limited to cancers involving RIBO R HSRIREM1 erythrocytes). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving erythrocytes. (The TF-1 cell line is a human erythroblast cell line available through the ATCC ™ as cell line number CRL-2003). 187 HFCCQ50 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) U937 BaxDHFR gb|AF250190|AF250190gb| such as described herein under the heading “Hyperproliferative M1 RIBO R V00507| Disordersî (particularly including, but not limited to, cancers of immune HSDHFRgb| cells, such as monocytes). Highly preferred embodiments of the X59543|HSRIREM1 invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving cells of the immune system (such as monocytes). (THe U-937 cell line is a human monocyte cell line available through the ATCC ™ as cell line number CRL-1593.2) 187 HFCCQ50 Immune Highly preferred indications include immunological disorders such as TF-1 CD40CD69 gb|AJ300189|HSA30018gb| described herein under the heading “Immune Activity” and/or “Blood- Z22576| Related Disorders” (particularly including, but not limited to, immune HSCD69GNA disorders involving erythrocytes). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving erythrocytes). (The TF-1 cell line is a human erythroblast cell line available through the ATCC ™ as cell line number CRL-2003). 187 HFCCQ50 Immune Highly preferred indications include immunological disorders such as U937 ICAMIRF1 gb|X06990|HSICAM1gb| described herein under the heading “Immune Activity” and/or “Blood- LTBR X14454| Related Disorders” (particularly including, but not limited to, immune HSIRF1gb|AK027080| disorders involving monocytes). Highly preferred embodiments of the AK027080 invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving monocytes). (The U937 cell line is a human monocyte cell line available through the ATCC ™ as cell line number CRL-1593.2). 188 HFCEW05 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) TF-1 c-junp21 gb|BC006175|BC006175gb| such as described herein under the heading “Hyperproliferative BC000275| Disordersî (particularly including, but not limited to cancers involving BC000275 erythrocytes). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving erythrocytes. (The TF-1 cell line is a human erythroblast cell line available through the ATCC ™ as cell line number CRL-2003). 188 HFCEW05 Immune Highly preferred indications include immunological disorders such as TF-1 CD40IL1B gb|AJ300189|HSA30018gb| described herein under the heading “Immune Activity” and/or “Blood- LTBR X02532| Related Disorders” (particularly including, but not limited to, immune HSIL1BRgb| disorders involving erythrocytes). Highly preferred embodiments of the AK027080|AK027080 invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving erythrocytes). (The TF-1 cell line is a human erythroblast cell line available through the ATCC ™ as cell line number CRL-2003). 204 HFVAB79 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, U937 ICAM gb|X06990|HSICAM1 and/or amelioration of diseases and disorders involving angiogenesis, wound healing, neoplasia (particularly including, but not limited to, tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(The U937 cell line is a human monocyte cell line available through the ATCC ™ as cell line number CRL-1593.2). 204 HFVAB79 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) U937 c-jun gb|BC006175|BC006175 such as described herein under the heading “Hyperproliferative Disordersî (particularly including, but not limited to, cancers of immune cells, such as monocytes). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving cells of the immune system (such as monocytes). (THe U-937 cell line is a human monocyte cell line available through the ATCC ™ as cell line number CRL-1593.2) 204 HFVAB79 Immune Highly preferred indications include immunological disorders such as U937 CTLA4IC gb|AF316875|AF316875gb| described herein under the heading “Immune Activity” and/or “Blood- AMLTBR X06990| Related Disorders” (particularly including, but not limited to, immune TNF HSICAM1gb| disorders involving monocytes). Highly preferred embodiments of the AK027080|AK027080gb| invention include methods of preventing, detecting, diagnosing, treating AJ270944| and/or ameliorating disorders of the immune system (particularly HSA27094 including, but not limited to, immune disorders involving monocytes). (The U937 cell line is a human monocyte cell line available through the ATCC ™ as cell line number CRL-1593.2). 249 HJACG02 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, Adipocytes- ICAMPAI gb|X06990|HSICAM1gb| and/or amelioration of diseases and disorders involving angiogenesis, Mar. 12, 2001 Vegf1 X12701| wound healing, neoplasia (particularly including, but not limited to, HSENDPAIgb| tumor metastases), and cardiovascular diseases and disorders; as AF024710|AF024710 described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.” 249 HJACG02 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, AOSMC VCAM gb|A30922|A30922 and/or amelioration of diseases and disorders involving angiogenesis, wound healing, neoplasia (particularly including, but not limited to, tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(AOSMC cells are aortic smooth muscle cells). 249 HJACG02 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, Daudi ICAMVCAM gb|X06990|HSICAM1gb| and/or amelioration of diseases and disorders involving angiogenesis, A30922| wound healing, neoplasia (particularly including, but not limited to, A30922 tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(The Daudi cell line is a human B lymphoblast cell line available through the ATCC ™ as cell line number CCL-213). 249 HJACG02 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, HUVEC ICAMTSP- gb|X06990|HSICAM1gb| and/or amelioration of diseases and disorders involving angiogenesis, 1Vegf1 X04665| wound healing, neoplasia (particularly including, but not limited to, HSTHROMRgb| tumor metastases), and cardiovascular diseases and disorders; as AF024710|AF024710 described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(HUVEC cells are human umbilical vein endothelial cells). 249 HJACG02 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) Adipocytes- Egr1 such as described herein under the heading “Hyperproliferative Mar. 12, 2001 Disordersî (particularly including, but not limited to, cancer involving adipocytes). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders. (Primary adipocytes) 249 HJACG02 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) AOSMC M1 RIBOR gb|X59543|HSRIREM1 such as described herein under the heading “Hyperproliferative Disordersî (particularly including, but not limited to, cancers of muscle tissues and the cardiovascular system (e.g. heart, lungs, circulatory system)). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders. (AOSMC cells are aortic smooth muscle cells). 249 HJACG02 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) Daudi Cyclin A1 gb|U97680|HSU97680 such as described herein under the heading “Hyperproliferative Disordersî (particularly including, but not limited to, cancers of immune cells, such as B-cells). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving immune cells (such as B-cells). (The Daudi cell line is a human B lymphoblast cell line available through the ATCC ™ as cell line number CCL-213). 249 HJACG02 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) HEK293 E-cadherin gb|Z35408|HSECAD9 such as described herein under the heading “Hyperproliferative Disordersî (particularly including, but not limited to, cancers of epithelial cells or cancers involving the renal system). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving epithelial cells or the renal system. (The 293 cell line human embryonal kidney epithelial cell line available through the ATCC ™ as cell line number CRL-1573). 249 HJACG02 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) Jurkat Cyclin A1 gb|U97680|HSU97680 such as described herein under the heading “Hyperproliferative Disordersî (particularly including, but not limited to, cancers of immune cells, such as T-cells). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving immune cells (such as T-cells). (The Jurkat cell line is a human T lymphocyte cell line available through the ATCC ™ as cell line number TIB-152). 249 HJACG02 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) Liver Cyclin D2 gb|X68452|HSCYCD2 such as described herein under the heading “Hyperproliferative Disordersî (particularly including, but not limited to, cancers involving cells of the hepatic system). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving cells of the hepatic system. 249 HJACG02 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) NHDF Cyclin A1 gb|U97680|HSU97680 such as described herein under the heading “Hyperproliferative Disordersî (particularly including, but not limited to cancers involving cells of the skin). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving skin cells. (NHDF cells are normal human dermal fibroblasts). 249 HJACG02 Immune Highly preferred indications include immunological disorders such as Adipocytes- ICAMI16Rag1 gb|X06990|HSICAM1gb| described herein under the heading “Immune Activity” and/or “Blood- Mar. 12, 2001 X04403| Related Disorders” (particularly including, but not limited to, immune HS26KDARgb| disorders involving adipocytes). Highly preferred embodiments of the M29474|HUMRAG1 invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving adipocytes). 249 HJACG02 Immune Highly preferred indications include immunological disorders such as AOSMC CD30CD4 gb|AJ300189|HSA30018gb| described herein under the heading “Immune Activity” and/or “Blood- 0IL1BIL5T X02532| Related Disorders” (particularly including, but not limited to, immune NFVCAM HSIL1BRgb| disorders involving muscle tissues and the cardiovascular system (e.g. X12705|HSBCDFIAgb| heart, lungs, circulatory system)). Highly preferred embodiments of the AJ270944| invention include methods of preventing, detecting, diagnosing, treating HSA27094gb| and/or ameliorating disorders of the immune system (particularly A30922|A30922 including, but not limited to, immune disorders involving muscle tissue or the cardiovascular system). (AOSMC cells are human aortic smooth muscle cells). 249 HJACG02 Immune Highly preferred indications include immunological disorders such as Caco-2 Rag1 gb|M29474|HUMRAG1 described herein under the heading “Immune Activity” and/or “Blood- Related Disorders” (particularly including, but not limited to, immune disorders involving the cells of the gastrointestinal tract). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving cells of the gastrointestinal tract). (The Caco-2 cell line is a human colorectal adenocarcinoma cell line available through the ATCC ™ as cell line number HTB-37). 249 HJACG02 Immune Highly preferred indications include immunological disorders such as Daudi ICAMRag1 gb|X06990|HSICAM1gb| described herein under the heading “Immune Activity” and/or “Blood- VCAM M29474| Related Disorders” (particularly including, but not limited to, immune HUMRAG1gb| disorders involving the B-cells). Highly preferred embodiments of the A30922|A30922 invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving B-cells). (The Daudi cell line is a human B lymphoblast cell line available through the ATCC ™ as cell line number CCL-213). 249 HJACG02 Immune Highly preferred indications include immunological disorders such as HEK293 c-maf gb|AF055377|AF055377 described herein under the heading “Immune Activity” and/or “Blood- Related Disorders” (particularly including, but not limited to, immune disorders involving epithelial cells or the renal system). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving epithelial cells or the renal system). (The 293 cell line is a human embryonal kidney epithelial cell line available through the ATCC ™ as cell line number CRL-1573). 249 HJACG02 Immune Highly preferred indications include immunological disorders such as HUVEC ICAM gb|X06990|HSICAM1 described herein under the heading “Immune Activity” and/or “Blood- Related Disorders” (particularly including, but not limited to, immune disorders involving endothelial cells). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving endothelial cells). (HUVEC cells are human umbilical vein endothelial cells). 249 HJACG02 Immune Highly preferred indications include immunological disorders such as Jurkat Rag2TNF gb|AY011962|AY011962gb| described herein under the heading “Immune Activity” and/or “Blood- AJ270944| Related Disorders” (particularly including, but not limited to, immune HSA27094 disorders involving T-cells). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving T-cells). (The Jurkat cell line is a human T lymphocyte cell line available through the ATCC ™ as cell line number TIB-152). 249 HJACG02 Immune Highly preferred indications include immunological disorders such as NHDF Rag1 gb|M29474|HUMRAG1 described herein under the heading “Immune Activity” and/or “Blood- Related Disorders” (particularly including, but not limited to, immune disorders involving the skin). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving the skin). (NHDF cells are normal human dermal fibroblasts). 249 HJACG02 Immune Highly preferred indications include immunological disorders such as U937 GATA1IL5 gb|X17254|HSERYF1gb| described herein under the heading “Immune Activity” and/or “Blood- TNF X12705| Related Disorders” (particularly including, but not limited to, immune HSBCDFIAgb| disorders involving monocytes). Highly preferred embodiments of the AJ270944|HSA27094 invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving monocytes). (The U937 cell line is a human monocyte cell line available through the ATCC ™ as cell line number CRL-1593.2). 265 HKACD58 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, AOSMC VCAMVeg gb|A30922|A30922gb| and/or amelioration of diseases and disorders involving angiogenesis, f1 AF024710| wound healing, neoplasia (particularly including, but not limited to, AF024710 tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(AOSMC cells are aortic smooth muscle cells). 265 HKACD58 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, HEK293 TSP- gb|X04665|HSTHROMRgb| and/or amelioration of diseases and disorders involving angiogenesis, 1Vegf1 AF024710| wound healing, neoplasia (particularly including, but not limited to, AF024710 tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(The HEK293 cell line is a human embryonal kidney epithelial cell line available through the ATCC ™ as cell line number CRL-1573). 265 HKACD58 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, HUVEC ICAM gb|X06990|HSICAM1 and/or amelioration of diseases and disorders involving angiogenesis, wound healing, neoplasia (particularly including, but not limited to, tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(HUVEC cells are human umbilical vein endothelial cells). 265 HKACD58 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, NHDF VCAM gb|A30922|A30922 and/or amelioration of diseases and disorders involving angiogenesis, wound healing, neoplasia (particularly including, but not limited to, tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(NHDF cells are normal human dermal fibroblasts). 265 HKACD58 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) AOSMC Cyclin D2 gb|X68452|HSCYCD2 such as described herein under the heading “Hyperproliferative Disordersî (particularly including, but not limited to, cancers of muscle tissues and the cardiovascular system (e.g. heart, lungs, circulatory system)). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders. (AOSMC cells are aortic smooth muscle cells). 265 HKACD58 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) Daudi c-jun gb|BC006175|BC006175 such as described herein under the heading “Hyperproliferative Disordersî (particularly including, but not limited to, cancers of immune cells, such as B-cells). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving immune cells (such as B-cells). (The Daudi cell line is a human B lymphoblast cell line available through the ATCC ™ as cell line number CCL-213). 265 HKACD58 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) HEK293 bcl- gb|X06487|HSBCL2IGgb| such as described herein under the heading “Hyperproliferative 2DHFRp21 V00507| Disordersî (particularly including, but not limited to, cancers of U66469 HSDHFRgb|BC000275| epithelial cells or cancers involving the renal system). Highly preferred p53 BC000275 embodiments of the invention include methods of preventing, detecting, regulated diagnosing, treating and/or ameliorating cancer and hyperproliferative gene disorders involving epithelial cells or the renal system. (The 293 cell line human embryonal kidney epithelial cell line available through the ATCC ™ as cell line number CRL-1573). 265 HKACD58 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) HUVEC U66469 such as described herein under the heading “Hyperproliferative p53 Disordersî (particularly including, but not limited to, cancers involving regulated endothelial cells). Highly preferred embodiments of the invention gene include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving endothelial cells. (HUVEC cells are human umbilical vein endothelial cells). 265 HKACD58 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) Jurkat Cyclin D2 gb|X68452|HSCYCD2 such as described herein under the heading “Hyperproliferative Disordersî (particularly including, but not limited to, cancers of immune cells, such as T-cells). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving immune cells (such as T-cells). (The Jurkat cell line is a human T lymphocyte cell line available through the ATCC ™ as cell line number TIB-152). 265 HKACD58 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) Liver Cyclin gb|AR034832|AR034832 such as described herein under the heading “Hyperproliferative D3Egr1 R034832 Disordersî (particularly including, but not limited to, cancers involving cells of the hepatic system). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving cells of the hepatic system. 265 HKACD58 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) THP1 Cyclin gb|BC000076|BC000076gb| such as described herein under the heading “Hyperproliferative Dp21 BC000275| Disordersî (particularly including, but not limited to, cancers of immune BC000275 cells, such as monocytes). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving cells of the immune system (such as monocytes). (The THP-1 cell line is a human monocyte cell line available through the ATCC ™ as cell line number TIB-202). 265 HKACD58 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) U937 c-junCyclin gb|BC006175|BC006175gb| such as described herein under the heading “Hyperproliferative A1 U97680| Disordersî (particularly including, but not limited to, cancers of immune HSU97680 cells, such as monocytes). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving cells of the immune system (such as monocytes). (The U-937 cell line is a human monocyte cell line available through the ATCC ™ as cell line number CRL-1593.2) 265 HKACD58 Immune Highly preferred indications include immunological disorders such as AOSMC VCAM gb|A30922|A30922 described herein under the heading “Immune Activity” and/or “Blood- Related Disorders” (particularly including, but not limited to, immune disorders involving muscle tissues and the cardiovascular system (e.g. heart, lungs, circulatory system)). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving muscle tissue or the cardiovascular system). (AOSMC cells are human aortic smooth muscle cells). 265 HKACD58 Immune Highly preferred indications include immunological disorders such as Daudi CD40 gb|AJ300189|HSA30018 described herein under the heading “Immune Activity” and/or “Blood- Related Disorders” (particularly including, but not limited to, immune disorders involving the B-cells). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving B-cells). (The Daudi cell line is a human B lymphoblast cell line available through the ATCC ™ as cell line number CCL-213). 265 HKACD58 Immune Highly preferred indications include immunological disorders such as HUVEC ICAMRag1 gb|X06990|HSICAM1gb| described herein under the heading “Immune Activity” and/or “Blood- M29474| Related Disorders” (particularly including, but not limited to, immune HUMRAG1 disorders involving endothelial cells). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving endothelial cells). (HUVEC cells are human umbilical vein endothelial cells). 265 HKACD58 Immune Highly preferred indications include immunological disorders such as Liver CD28 gb|AF222342|AF222342 described herein under the heading “Immune Activity” and/or “Blood- Related Disorders” (particularly including, but not limited to, immune disorders involving cells of the hepatic system). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving cells of the hepatic system). 265 HKACD58 Immune Highly preferred indications include immunological disorders such as NHDF CXCR3GA gb|Z79783|HSCKRL2gb| described herein under the heading “Immune Activity” and/or “Blood- TA1Il6VCAM X17254| Related Disorders” (particularly including, but not limited to, immune HSERYF1gb| disorders involving the skin). Highly preferred embodiments of the X04403|HS26KDARgb| invention include methods of preventing, detecting, diagnosing, treating A30922| and/or ameliorating disorders of the immune system (particularly A30922 including, but not limited to, immune disorders involving the skin). (NHDF cells are normal human dermal fibroblasts). 265 HKACD58 Immune Highly preferred indications include immunological disorders such as THP1 CIS3 gb|AB006967|AB006967 described herein under the heading “Immune Activity” and/or “Blood- Related Disorders” (particularly including, but not limited to, immune disorders involving monocytes). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving monocytes). (The THP1 cell line is a human monocyte cell line available through the ATCC ™ as cell line number TIB-202). 265 HKACD58 Immune Highly preferred indications include immunological disorders such as U937 CD69TNF gb|Z22576|HSCD69GNAgb| described herein under the heading “Immune Activity” and/or “Blood- AJ270944| Related Disorders” (particularly including, but not limited to, immune HSA27094 disorders involving monocytes). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving monocytes). (The U937 cell line is a human monocyte cell line available through the ATCC ™ as cell line number CRL-1593.2). 281 HL2AC08 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) TF-1 p21 gb|BC000275|BC000275 such as described herein under the heading “Hyperproliferative Disordersî (particularly including, but not limited to cancers involving erythrocytes). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving erythrocytes. (The TF-1 cell line is a human erythroblast cell line available through the ATCC ™ as cell line number CRL-2003). 281 HL2AC08 Immune Highly preferred indications include immunological disorders such as TF-1 CD69GAT gb|Z22576|HSC D69GNAgb| described herein under the heading “Immune Activity” and/or “Blood- A1TNF X17254| Related Disorders” (particularly including, but not limited to, immune HSERYF1gb| disorders involving erythrocytes). Highly preferred embodiments of the AJ270944|HSA27094 invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving erythrocytes). (The TF-1 cell line is a human erythroblast cell line available through the ATCC ™ as cell line number CRL-2003). 389 HNHFO29 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, U937 Flt1ICAM gb|AF063657|AF063657gb| and/or amelioration of diseases and disorders involving angiogenesis, PAI X06990| wound healing, neoplasia (particularly including, but not limited to, HSICAM1gb| tumor metastases), and cardiovascular diseases and disorders; as X12701|HSENDPAI described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(The U937 cell line is a human monocyte cell line available through the ATCC ™ as cell line number CRL-1593.2). 389 HNHFO29 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) TF-1 bcl-2Cyclin gb|X06487|HSBCL2IGgb| such as described herein under the heading “Hyperproliferative DDHFREgr1 BC000076| Disordersî (particularly including, but not limited to cancers involving BC000076gb| erythrocytes). Highly preferred embodiments of the invention include V00507|HSDHFR methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving erythrocytes. (The TF-1 cell line is a human erythroblast cell line available through the ATCC ™ as cell line number CRL-2003). 389 HNHFO29 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) U937 Cyclin gb|BC000076|BC000076gb| such as described herein under the heading “Hyperproliferative DCyclin AR034832| Disordersî (particularly including, but not limited to, cancers of immune D3DHFR AR034832gb| cells, such as monocytes). Highly preferred embodiments of the V00507|HSDHFR invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving cells of the immune system (such as monocytes). (THe U-937 cell line is a human monocyte cell line available through the ATCC ™ as cell line number CRL-1593.2) 389 HNHFO29 Immune Highly preferred indications include immunological disorders such as TF-1 CD40TNF gb|AJ300189|HSA3018gb| described herein under the heading “Immune Activity” and/or “Blood- AJ270944| Related Disorders” (particularly including, but not limited to, immune HSA27094 disorders involving erythrocytes). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving erythrocytes). (The TF-1 cell line is a human erythroblast cell line available through the ATCC ™ as cell line number CRL-2003). 389 HNHFO29 Immune Highly preferred indications include immunological disorders such as U937 ICAM gb|X06990|HSICAM1 described herein under the heading “Immune Activity” and/or “Blood- Related Disorders” (particularly including, but not limited to, immune disorders involving monocytes). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving monocytes). (The U937 cell line is a human monocyte cell line available through the ATCC ™ as cell line number CRL-1593.2). 495 HSDSB09 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, AOSMC VCAM gb|A30922|A30922 and/or amelioration of diseases and disorders involving angiogenesis, wound healing, neoplasia (particularly including, but not limited to, tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(AOSMC cells are aortic smooth muscle cells). 495 HSDSB09 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, Caco-2 ICAMVegf1 gb|X06990|HSICAM1gb| and/or amelioration of diseases and disorders involving angiogenesis, AF024710| wound healing, neoplasia (particularly including, but not limited to, AF024710 tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(The Caco-2 cell line is a human colorectal adenocarcinoma cell line available through the ATCC ™ as cell line number HTB-37). 495 HSDSB09 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, HEK293 CyclooxVCAM gb|A30922|A30922 and/or amelioration of diseases and disorders involving angiogenesis, wound healing, neoplasia (particularly including, but not limited to, tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(The HEK293 cell line is a human embryonal kidney epithelial cell line available through the ATCC ™ as cell line number CRL-1573). 495 HSDSB09 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, HUVEC ICAMVegf1 gb|X06990|HSICAM1gb| and/or amelioration of diseases and disorders involving angiogenesis, AF024710| wound healing, neoplasia (particularly including, but not limited to, AF024710 tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(HUVEC cells are human umbilical vein endothelial cells). 495 HSDSB09 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, Jurkat Flt1 gb|AF063657|AF063657 and/or amelioration of diseases and disorders involving angiogenesis, wound healing, neoplasia (particularly including, but not limited to, tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(The Jurkat cell line is a human T lymphocyte cell line available through the ATCC ™ as cell line number TIB-152). 495 HSDSB09 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, Molt4 iNOS gb|X85761|HSNOS2E3 and/or amelioration of diseases and disorders involving angiogenesis, wound healing, neoplasia (particularly including, but not limited to, tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(The Molt4 cell line is a human T cell line available through the ATCC ™ as cell line number CRL-1582). 495 HSDSB09 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, NHDF Vegf1 gb|AF024710|AF024710 and/or amelioration of diseases and disorders involving angiogenesis, wound healing, neoplasia (particularly including, but not limited to, tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(NHDF cells are normal human dermnal fibroblasts). 495 HSDSB09 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, SUPT VCAM gb|A30922|A30922 and/or amelioration of diseases and disorders involving angiogenesis, wound healing, neoplasia (particularly including, but not limited to, tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(SUPT cells are human T-cells). 495 HSDSB09 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, THP1 ICAMTSP- gb|X06990|HSICAM1gb| and/or amelioration of diseases and disorders involving angiogenesis, 1VCAMVegf1 X04665| wound healing, neoplasia (particularly including, but not limited to, HSTHROMRgb| tumor metastases), and cardiovascular diseases and disorders; as A30922|A30922gb| described herein under the headings “Hyperproliferative Disorders,” AF024710| “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular AF024710 Level,” and “Wound Healing and Epithelial Cell Proliferation.”(The THP-1 cell line is a human monocyte cell line available through the ATCC ™ as cell line number TIB-202). 495 HSDSB09 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) AOSMC bcl-2Cyclin gb|X06487|HSBCL2IGgb| such as described herein under the heading “Hyperproliferative A1M1 U97680| Disordersî (particularly including, but not limited to, cancers of muscle RIBO R HSU97680gb| tissues and the cardiovascular system (e.g. heart, lungs, circulatory X59543|HSRIREM1 system)). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders. (AOSMC cells are aortic smooth muscle cells). 495 HSDSB09 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) Caco-2 DHFREgr1 gb|V00507|HSDHFRgb| such as described herein under the heading “Hyperproliferative p53U66469 X60011| Disordersî (particularly including, but not limited to, cancer involving p53 HSP53002 cells of the gastrointestinal tract). Highly preferred embodiments of the regulated invention include methods of preventing, detecting, diagnosing, treating gene and/or ameliorating cancer and hyperproliferative disorders involving the gastrointestinal tract. (The Caco-2 cell line is a human colorectal adenocarcinoma cell line available through the ATCC ™ as cell line number HTB-37). 495 HSDSB09 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) H9 DHFRU66 gb|V00507|HSDHFR such as described herein under the heading “Hyperproliferative 469 p53 Disordersî (particularly including, but not limited to, cancers of immune regulated cells, such as T-cells). Highly preferred embodiments of the invention gene include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving immune cells (such as T-cells). (The H9 cell line is a human T lymphocyte cell line available through the ATCC ™ as cell line number HTB-176). 495 HSDSB09 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) HEK293 bcl-2Cyclin gb|X06487|HSBCL2IGgb| such as described herein under the heading “Hyperproliferative DE- BC000076| Disordersî (particularly including, but not limited to, cancers of cadherinM BC000076gb| epithelial cells or cancers involving the renal system). Highly preferred 1 RIBO R Z35408|HSECAD9gb| embodiments of the invention include methods of preventing, detecting, X59543| diagnosing, treating and/or ameliorating cancer and hyperproliferative HSRIREM1 disorders involving epithelial cells or the renal system. (The 293 cell line human embryonal kidney epithelial cell line available through the ATCC ™ as cell line number CRL-1573). 495 HSDSB09 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) HUVEC Cyclin D2 gb|X68452|HSCYCD2 such as described herein under the heading “Hyperproliferative Disordersî (particularly including, but not limited to, cancers involving endothelial cells). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving endothelial cells. (HUVEC cells are human umbilical vein endothelial cells). 495 HSDSB09 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) Jurkat Cyclin gb|U97680|HSU97680gb| such as described herein under the heading “Hyperproliferative A1Cyclin BC000076| Disordersî (particularly including, but not limited to, cancers of immune DCyclin BC000076gb| cells, such as T-cells). Highly preferred embodiments of the invention D2Cyclin X68452|HSCYCD2gb| include methods of preventing, detecting, diagnosing, treating and/or D3DHFRE AR034832| ameliorating cancer and hyperproliferative disorders involving immune gr1 AR034832gb| cells (such as T-cells). (The Jurkat cell line is a human T lymphocyte V00507|HSDHFR cell line available through the ATCC ™ as cell line number TIB-152). 495 HSDSB09 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) Liver Cyclin gb|X68452|HSCYCD2gb| such as described herein under the heading “Hyperproliferative D2DHFR V00507| Disordersî (particularly including, but not limited to, cancers involving HSDHFR cells of the hepatic system). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving cells of the hepatic system. 495 HSDSB09 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) Molt4 Cyclin gb|X68452|HSCYCD2gb| such as described herein under the heading “Hyperproliferative D2p21 BC000275| Disordersî (particularly including, but not limited to, cancers of immune BC000275 cells, such as T-cells). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving immune cells (such as T-cells). (The Molt-4 cell line is a human T-cell line available through the ATCC ™ as cell line number CRL-1582). 495 HSDSB09 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) NHDF U66469 such as described herein under the heading “Hyperproliferative p53 Disordersî (particularly including, but not limited to cancers involving regulated cells of the skin). Highly preferred embodiments of the invention gene include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving skin cells. (NHDF cells are normal human dermal fibroblasts). 495 HSDSB09 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) SK-N- Cyclin gb|U97680|HSU97680gb| such as described herein under the heading “Hyperproliferative MC A1Egr1p53 X60011| Disordersî (particularly including, but not limited to cancers involving neuroblastoma U66469 HSP53002 cells of the brain/central nervous system (e.g. neural epithelium)). p53 Highly preferred embodiments of the invention include methods of regulated preventing, detecting, diagnosing, treating and/or ameliorating cancer gene and hyperproliferative disorders involving the brain or central nervous system. (The SK-N-MC neuroblastoma cell line is a cell line derived from human brain tissue available through the ATCC ™ as cell line number HTB-10). 495 HSDSB09 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) THP1 Cyclin gb|BC000076|BC000076gb| such as described herein under the heading “Hyperproliferative DDHFREg V00507| Disordersî (particularly including, but not limited to, cancers of immune r1p21U664 HSDHFRgb| cells, such as monocytes). Highly preferred embodiments of the 69 p53 BC000275|BC000275 invention include methods of preventing, detecting, diagnosing, treating regulated and/or ameliorating cancer and hyperproliferative disorders involving gene cells of the immune system (such as monocytes). (The THP-1 cell line is a human monocyte cell line available through the ATCC ™ as cell line number TIB-202). 495 HSDSB09 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) U937 Egr1 such as described herein under the heading “Hyperproliferative Disordersî (particularly including, but not limited to, cancers of immune cells, such as monocytes). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving cells of the immune system (such as monocytes). (The U-937 cell line is a human monocyte cell line available through the ATCC ™ as cell line number CRL-1593.2) 495 HSDSB09 Immune Highly preferred indications include immunological disorders such as AOSMC CCR3CCR gb|AB023887|AB023887gb| described herein under the heading “Immune Activity” and/or “Blood- 4CD25CD AB023888| Related Disorders” (particularly including, but not limited to, immune 30CD40CT AB023888gb| disorders involving muscle tissues and the cardiovascular system (e.g. LA4IL5Ra X03137|HSIL2RG7gb| heart, lungs, circulatory system)). Highly preferred embodiments of the g1VCAM AJ300189| invention include methods of preventing, detecting, diagnosing, treating HSA30018gb| and/or ameliorating disorders of the immune system (particularly AF316875|AF316875gb| including, but not limited to, immune disorders involving muscle tissue X12705| or the cardiovascular system). (AOSMC cells are human aortic smooth HSBCDFIAgb| muscle cells). M29474|HUMRAG1gb| A30922| A30922 495 HSDSB09 Immune Highly preferred indications include immunological disorders such as Caco-2 c- gb|AF055377|AF055377gb| described herein under the heading “Immune Activity” and/or “Blood- mafGATA X55037| Related Disorders” (particularly including, but not limited to, immune 3ICAMRag1 HSGATA3gb| disorders involving the cells of the gastrointestinal tract). Highly X06990|HSICAM1gb| preferred embodiments of the invention include methods of preventing, M29474| detecting, diagnosing, treating and/or ameliorating disorders of the HUMRAG1 immune system (particularly including, but not limited to, immune disorders involving cells of the gastrointestinal tract). (The Caco-2 cell line is a human colorectal adenocarcinoma cell line available through the ATCC ™ as cell line number HTB-37). 495 HSDSB09 Immune Highly preferred indications include immunological disorders such as Daudi TNF gb|AJ270944|HSA27094 described herein under the heading “Immune Activity” and/or “Blood- Related Disorders” (particularly including, but not limited to, immune disorders involving the B-cells). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving B-cells). (The Daudi cell line is a human B lymphoblast cell line available through the ATCC ™ as cell line number CCL-213). 495 HSDSB09 Immune Highly preferred indications include immunological disorders such as H9 CIS3Rag1 gb|AB006967|AB006967gb| described herein under the heading “Immune Activity” and/or “Blood- M29474| Related Disorders” (particularly including, but not limited to, immune HUMRAG1 disorders involving the T-cells). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving T-cells). (The H9 cell line is a human T lymphocyte cell line available through the ATCC ™ as cell line number HTB-176). 495 HSDSB09 Immune Highly preferred indications include immunological disorders such as HEK293 CCR3CCR gb|AB023887|AB023887gb| described herein under the heading “Immune Activity” and/or “Blood- 4CD25CD AB023888| Related Disorders” (particularly including, but not limited to, immune 30CD40CT AB023888gb| disorders involving epithelial cells or the renal system). Highly LA4GATA X03137|HSIL2RG7gb| preferred embodiments of the invention include methods of preventing, 3Rag1TNF AJ300189| detecting, diagnosing, treating and/or ameliorating disorders of the VCAM HSA30018gb| immune system (particularly including, but not limited to, immune AF316875|AF316875gb| disorders involving epithelial cells or the renal system). (The 293 cell X55037| line is a human embryonal kidney epithelial cell line available through HSGATA3gb| the ATCC ™ as cell line number CRL-1573). M29474|HUMRAG1gb| AJ270944| HSA27094gb| A30922|A30922 495 HSDSB09 Immune Highly preferred indications include immunological disorders such as HUVEC CD40ICA gb|AJ300189|HSA30018gb| described herein under the heading “Immune Activity” and/or “Blood- MIL10Rag X06990| Related Disorders” (particularly including, but not limited to, immune 1Rag2TNF HSICAM1gb| disorders involving endothelial cells). Highly preferred embodiments AF055467|AF055467gb| of the invention include methods of preventing, detecting, diagnosing, M29474| treating and/or ameliorating disorders of the immune system HUMRAG1gb| (particularly including, but not limited to, immune disorders involving AY011962|AY011962gb| endothelial cells). (HUVEC cells are human umbilical vein endothelial AJ270944| cells). HSA27094 495 HSDSB09 Immune Highly preferred indications include immunological disorders such as Jurkat CD69IL5R gb|Z22576|HSCD69GNAgb| described herein under the heading “Immune Activity” and/or “Blood- antesTNF X12705| Related Disorders” (particularly including, but not limited to, immune HSBCDFIAgb| disorders involving T-cells). Highly preferred embodiments of the AF043341| invention include methods of preventing, detecting, diagnosing, treating AF043341gb|AJ270944| and/or ameliorating disorders of the immune system (particularly HSA27094 including, but not limited to, immune disorders involving T-cells). (The Jurkat cell line is a human T lymphocyte cell line available through the ATCC ™ as cell line number TIB-152). 495 HSDSB09 Immune Highly preferred indications include immunological disorders such as Liver CD25 gb|X03137|HSIL2RG7 described herein under the heading “Immune Activity” and/or “Blood- Related Disorders” (particularly including, but not limited to, immune disorders involving cells of the hepatic system). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving cells of the hepatic system). 495 HSDSB09 Immune Highly preferred indications include immunological disorders such as Molt4 CD28 gb|AF222342|AF222342 described herein under the heading “Immune Activity” and/or “Blood- Related Disorders” (particularly including, but not limited to, immune disorders involving T-cells). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving T-cells). (The Molt-4 cell line is a human T-cell line available through the ATCC ™ as cell line number CRL-1582). 495 HSDSB09 Immune Highly preferred indications include immunological disorders such as NHDF CD28CD40 gb|AF222342|AF222342gb| described herein under the heading “Immune Activity” and/or “Blood- I16 AJ300189| Related Disorders” (particularly including, but not limited to, immune HSA30018gb| disorders involving the skin). Highly preferred embodiments of the X04403|HS26KDAR invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving the skin). (NHDF cells are normal human dermal fibroblasts). 495 HSDSB09 Immune Highly preferred indications include immunological disorders such as SK-N- c- gb|AF055377|AF055377gb| described herein under the heading “Immune Activity” and/or “Blood- MC mafCIS3T AB006967| Related Disorders” (particularly including, but not limited to, immune neuroblastoma NF AB006967gb| disorders involving the central nervous system). Highly preferred AJ270944|HSA27094 embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving the central nervous sytem). (The SK-N-MC neuroblastoma cell line is a cell line derived from human brain tissue and is available through the ATCC ™ as cell line number HTB-10). 495 HSDSB09 Immune Highly preferred indications include immunological disorders such as SUPT TNFVCAM gb|AJ270944|HSA27094gb| described herein under the heading “Immune Activity” and/or “Blood- A30922| Related Disorders” (particularly including, but not limited to, immune A30922 disorders involving T-cells). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving T-cells). (The SUPT cell line is a human T-cell line). 495 HSDSB09 Immune Highly preferred indications include immunological disorders such as THP1 CCR3CD40 gb|AB023887|AB023887gb| described herein under the heading “Immune Activity” and/or “Blood- GATA3I AJ300189| Related Disorders” (particularly including, but not limited to, immune CAMIL5R HSA30018gb| disorders involving monocytes). Highly preferred embodiments of the ag2VCAM X55037|HSGATA3gb| invention include methods of preventing, detecting, diagnosing, treating X06990| and/or ameliorating disorders of the immune system (particularly HSICAM1gb| including, but not limited to, immune disorders involving monocytes). X12705|HSBCDFIAgb| (The THP1 cell line is a human monocyte cell line available through the AY011962| ATCC ™ as cell line number TIB-202). AY011962gb| A30922|A30922 495 HSDSB09 Immune Highly preferred indications include immunological disorders such as U937 IL1B gb|X02532|HSIL1BR described herein under the heading “Immune Activity” and/or “Blood- Related Disorders” (particularly including, but not limited to, immune disorders involving monocytes). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving monocytes). (The U937 cell line is a human monocyte cell line available through the ATCC ™ as cell line number CRL-1593.2). 596 HUKBT29 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) TF-1 p21 gb|BC000275|BC000275 such as described herein under the heading “Hyperproliferative Disordersî (particularly including, but not limited to cancers involving erythrocytes). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving erythrocytes. (The TF-1 cell line is a human erythroblast cell line available through the ATCC ™ as cell line number CRL-2003). 596 HUKBT29 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) U937 p21 gb|BC000275|BC000275 such as described herein under the heading “Hyperproliferative Disordersî (particularly including, but not limited to, cancers of immune cells, such as monocytes). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving cells of the immune system (such as monocytes). (THe U-937 cell line is a human monocyte cell line available through the ATCC ™ as cell line number CRL-1593.2) 596 HUKBT29 Immune Highly preferred indications include immunological disorders such as U937 CD69 gb|Z22576|HSCD69GNA described herein under the heading “Immune Activity” and/or “Blood- Related Disorders” (particularly including, but not limited to, immune disorders involving monocytes). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving monocytes). (The U937 cell line is a human monocyte cell line available through the ATCC ™ as cell line number CRL-1593.2). 615 HWHGZ51 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, AOSMC TSP-1 gb|X04665|HSTHROMR and/or amelioration of diseases and disorders involving angiogenesis, wound healing, neoplasia (particularly including, but not limited to, tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(AOSMC cells are aortic smooth muscle cells). 615 HWHGZ51 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, Daudi ICAMPAI gb|X06990|HSICAM1gb| and/or amelioration of diseases and disorders involving angiogenesis, X12701| wound healing, neoplasia (particularly including, but not limited to, HSENDPAI tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(The Daudi cell line is a human B lymphoblast cell line available through the ATCC ™ as cell line number CCL-213). 615 HWHGZ51 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, H9 VCAM gb|A30922|A30922 and/or amelioration of diseases and disorders involving angiogenesis, wound healing, neoplasia (particularly including, but not limited to, tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(The H9 cell line is a human T lymphocyte cell line available through the ATCC ™ as cell line number HTB-176). 615 HWHGZ51 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, HEK293 Flt1iNOS gb|AF063657|AF063657gb| and/or amelioration of diseases and disorders involving angiogenesis, X85761| wound healing, neoplasia (particularly including, but not limited to, HSNOS2E3 tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(The HEK293 cell line is a human embryonal kidney epithelial cell line available through the ATCC ™ as cell line number CRL-1573). 615 HWHGZ51 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, HUVEC Vegf1 gb|AF024710|AF024710 and/or amelioration of diseases and disorders involving angiogenesis, wound healing, neoplasia (particularly including, but not limited to, tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(HUVEC cells are human umbilical vein endothelial cells). 615 HWHGZ51 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, Liver Flt1ICAM gb|AF063657|AF063657gb| and/or amelioration of diseases and disorders involving angiogenesis, PAIVCAM X06990| wound healing, neoplasia (particularly including, but not limited to, HSICAM1gb| tumor metastases), and cardiovascular diseases and disorders; as X12701|HSENDPAIgb| described herein under the headings “Hyperproliferative Disorders,” A30922| “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular A30922 Level,” and “Wound Healing and Epithelial Cell Proliferation.” 615 HWHGZ51 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, Molt4 VCAM gb|A30922|A30922 and/or amelioration of diseases and disorders involving angiogenesis, wound healing, neoplasia (particularly including, but not limited to, tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(The Molt4 cell line is a human T cell line available through the ATCC ™ as cell line number CRL-1582). 615 HWHGZ51 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, NHDF Vegf1 gb|AF024710|AF024710 and/or amelioration of diseases and disorders involving angiogenesis, wound healing, neoplasia (particularly including, but not limited to, tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(NHDF cells are normal human dermal fibroblasts). 615 HWHGZ51 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, THP1 Vegf1 gb|AF024710|AF024710 and/or amelioration of diseases and disorders involving angiogenesis, wound healing, neoplasia (particularly including, but not limited to, tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(The THP-1 cell line is a human monocyte cell line available through the ATCC ™ as cell line number TIB-202). 615 HWHGZ51 Angiogenesis Highly preferred indications include diagnosis, prevention, treatment, U937 ICAMVegf1 gb|X06990|HSICAM1gb| and/or amelioration of diseases and disorders involving angiogenesis, AF024710| wound healing, neoplasia (particularly including, but not limited to, AF024710 tumor metastases), and cardiovascular diseases and disorders; as described herein under the headings “Hyperproliferative Disorders,” “Regeneration,” “Anti-Angiogenesis Activity,” “Diseases at the Cellular Level,” and “Wound Healing and Epithelial Cell Proliferation.”(The U937 cell line is a human monocyte cell line available through the ATCC ™ as cell line number CRL-1593.2). 615 HWHGZ51 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) AOSMC Cyclin gb|U97680|HSU97680gb| such as described herein under the heading “Hyperproliferative A1DHFR V00507| Disordersî (particularly including, but not limited to, cancers of muscle HSDHFR tissues and the cardiovascular system (e.g. heart, lungs, circulatory system)). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders. (AOSMC cells are aortic smooth muscle cells). 615 HWHGZ51 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) Caco-2 c-fosCyclin gb|BC004490|BC004490gb| such as described herein under the heading “Hyperproliferative A1 U97680| Disordersî (particularly including, but not limited to, cancer involving HSU97680 cells of the gastrointestinal tract). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving the gastrointestinal tract. (The Caco-2 cell line is a human colorectal adenocarcinoma cell line available through the ATCC ™ as cell line number HTB-37). 615 HWHGZ51 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) Daudi Bax gb|AF250190|AF250190 such as described herein under the heading “Hyperproliferative Disordersî (particularly including, but not limited to, cancers of immune cells, such as B-cells). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving immune cells (such as B-cells). (The Daudi cell line is a human B lymphoblast cell line available through the ATCC ™ as cell line number CCL-213). 615 HWHGZ51 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) HEK293 c-jun gb|BC006175|BC006175 such as described herein under the heading “Hyperproliferative Disordersî (particularly including, but not limited to, cancers of epithelial cells or cancers involving the renal system). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving epithelial cells or the renal system. (The 293 cell line human embryonal kidney epithelial cell line available through the ATCC ™ as cell line number CRL-1573). 615 HWHGZ51 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) HUVEC bcl-2TAA6 gb|X06487|HSBCL2IGgb| such as described herein under the heading “Hyperproliferative I34297| Disordersî (particularly including, but not limited to, cancers involving I34297 endothelial cells). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving endothelial cells. (HUVEC cells are human umbilical vein endothelial cells). 615 HWHGZ51 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) Liver Cyclin gb|AR034832|AR034832gb| such as described herein under the heading “Hyperproliferative D3M1 X59543| Disordersî (particularly including, but not limited to, cancers involving RIBO HSRIREM1 cells of the hepatic system). Highly preferred embodiments of the RU66469 invention include methods of preventing, detecting, diagnosing, treating p53 and/or ameliorating cancer and hyperproliferative disorders involving regulated cells of the hepatic system. gene 615 HWHGZ51 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) NHDF bcl-2TAA6 gb|X06487|HSBCL2IGgb| such as described herein under the heading “Hyperproliferative I34297| Disordersî (particularly including, but not limited to cancers involving I34297 cells of the skin). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving skin cells. (NHDF cells are normal human dermal fibroblasts). 615 HWHGZ51 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) THP1 DHFRM1 gb|V00507|HSDHFRgb| such as described herein under the heading “Hyperproliferative RIBO R X59543| Disordersî (particularly including, but not limited to, cancers of immune HSRIREM1 cells, such as monocytes). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving cells of the immune system (such as monocytes). (The THP-1 cell line is a human monocyte cell line available through the ATCC ™ as cell line number TIB-202). 615 HWHGZ51 Cancer Highly preferred indications include neoplastic diseases (e.g. cancer) U937 Cyclin A1 gb|U97680|HSU97680 such as described herein under the heading “Hyperproliferative Disordersî (particularly including, but not limited to, cancers of immune cells, such as monocytes). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating cancer and hyperproliferative disorders involving cells of the immune system (such as monocytes). (The U-937 cell line is a human monocyte cell line available through the ATCC ™ as cell line number CRL-1593.2) 615 HWHGZ51 Diabetes A highly preferred indication is diabetes. Additional highly preferred Liver GAPDH indications include complications associated with diabetes (e.g., diabetic retinopathy, diabetic nephropathy, kidney disease (e.g., renal failure, nephropathy and/or other diseases and disorders as described in the “Renal Disorders” section below), diabetic neuropathy, nerve disease and nerve damage (e.g., due to diabetic neuropathy), blood vessel blockage, heart disease, stroke, impotence (e.g., due to diabetic neuropathy or blood vessel blockage), seizures, mental confusion, drowsiness, nonketotic hyperglycemic-hyperosmolar coma, cardiovascular disease (e.g., heart disease, atherosclerosis, microvascular disease, hypertension, stroke, and other diseases and disorders as described in the “Cardiovascular Disorders” section below), dyslipidemia, endocrine disorders (as described in the “Endocrine Disorders” section below), neuropathy, vision impairment (e.g., diabetic retinopathy and blindness), ulcers and impaired wound healing, and infection (e.g., infectious diseases and disorders as described in the “Infectious Diseases” section below, especially of the urinary tract and skin). Highly preferred indications also include obesity, weight gain, and weight loss, as well as complications associated with obesity, weight gain, and weight loss. Preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating the above mentioned conditions, disorders, and diseases. 615 HWHGZ51 Immune Highly preferred indications include immunological disorders such as AOSMC CD30I16 gb|X04403|HS26KDAR described herein under the heading “Immune Activity” and/or “Blood- Related Disorders” (particularly including, but not limited to, immune disorders involving muscle tissues and the cardiovascular system (e.g. heart, lungs, circulatory system)). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving muscle tissue or the cardiovascular system). (AOSMC cells are human aortic smooth muscle cells). 615 HWHGZ51 Immune Highly preferred indications include immunological disorders such as Caco-2 Rag1 gb|M29474|HUMRAG1 described herein under the heading “Immune Activity” and/or “Blood- Related Disorders” (particularly including, but not limited to, immune disorders involving the cells of the gastrointestinal tract). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving cells of the gastrointestinal tract). (The Caco-2 cell line is a human colorectal adenocarcinoma cell line available through the ATCC ™ as cell line number HTB-37). 615 HWHGZ51 Immune Highly preferred indications include immunological disorders such as Daudi CIS3CXC gb|AB006967|AB006967gb| described herein under the heading “Immune Activity” and/or “Blood- R3ICAM Z79783| Related Disorders” (particularly including, but not limited to, immune HSCKRL2gb| disorders involving the B-cells). Highly preferred embodiments of the X06990|HSICAM1 invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving B-cells). (The Daudi cell line is a human B lymphoblast cell line available through the ATCC ™ as cell line number CCL-213). 615 HWHGZ51 Immune Highly preferred indications include immunological disorders such as H9 IL5VCAM gb|X12705|HSBCDFIAgb| described herein under the heading “Immune Activity” and/or “Blood- VLA4 A30922| Related Disorders” (particularly including, but not limited to, immune A30922gb|X16983| disorders involving the T-cells). Highly preferred embodiments of the HSINTAL4 invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving T-cells). (The H9 cell line is a human T lymphocyte cell line available through the ATCC ™ as cell line number HTB-176). 615 HWHGZ51 Immune Highly preferred indications include immunological disorders such as HEK293 Rag1TNF gb|M29474|HUMRAG1gb| described herein under the heading “Immune Activity” and/or “Blood- AJ270944| Related Disorders” (particularly including, but not limited to, immune HSA27094 disorders involving epithelial cells or the renal system). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving epithelial cells or the renal system). (The 293 cell line is a human embryonal kidney epithelial cell line available through the ATCC ™ as cell line number CRL-1573). 615 HWHGZ51 Immune Highly preferred indications include immunological disorders such as HUVEC CCR7GAT gb|X84702|HSDNABLR2gb| described herein under the heading “Immune Activity” and/or “Blood- A3TNF X55037| Related Disorders” (particularly including, but not limited to, immune HSGATA3gb| disorders involving endothelial cells). Highly preferred embodiments AJ270944|HSA27094 of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving endothelial cells). (HUVEC cells are human umbilical vein endothelial cells). 615 HWHGZ51 Immune Highly preferred indications include immunological disorders such as Jurkat Rag1Rag2 gb|M29474|HUMRAG1gb| described herein under the heading “Immune Activity” and/or “Blood- AY011962| Related Disorders” (particularly including, but not limited to, immune AY011962 disorders involving T-cells). Highly preferred embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving T-cells). (The Jurkat cell line is a human T lymphocyte cell line available through the ATCC ™ as cell line number TIB-152). 615 HWHGZ51 Immune Highly preferred indications include immunological disorders such as Liver CCR7ICA gb|X84702|HSDNABLR2gb| described herein under the heading “Immune Activity” and/or “Blood- MTNFVC X06990| Related Disorders” (particularly including, but not limited to, immune AM HSICAM1gb| disorders involving cells of the hepatic system). Highly preferred AJ270944|HSA27094gb| embodiments of the invention include methods of preventing, detecting, A30922| diagnosing, treating and/or ameliorating disorders of the immune A30922 system (particularly including, but not limited to, immune disorders involving cells of the hepatic system). 615 HWHGZ51 Immune Highly preferred indications include immunological disorders such as Molt4 CD25TNF gb|X03137|HSIL2RG7gb| described herein under the heading “Immune Activity” and/or “Blood- VCAM AJ270944| Related Disorders” (particularly including, but not limited to, immune HSA27094gb| disorders involving T-cells). Highly preferred embodiments of the A30922|A30922 invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving T-cells). (The Molt-4 cell line is a human T-cell line available through the ATCC ™ as cell line number CRL-1582). 615 HWHGZ51 Immune Highly preferred indications include immunological disorders such as NHDF CCR7CD40 gb|X84702|HSDNABLR2gb| described herein under the heading “Immune Activity” and/or “Blood- GATA3H AJ300189| Related Disorders” (particularly including, but not limited to, immune LA-cTNF HSA30018gb| disorders involving the skin). Highly preferred embodiments of the X55037|HSGATA3gb| invention include methods of preventing, detecting, diagnosing, treating AJ270944| and/or ameliorating disorders of the immune system (particularly HSA27094 including, but not limited to, immune disorders involving the skin). (NHDF cells are normal human dermal fibroblasts). 615 HWHGZ51 Immune Highly preferred indications include immunological disorders such as SK-N- CIS3LTBR gb|AB006967|AB006967gb| described herein under the heading “Immune Activity” and/or “Blood- MC Rag1 AK027080| Related Disorders” (particularly including, but not limited to, immune neuroblastoma AK027080gb| disorders involving the central nervous system). Highly preferred M29474|HUMRAG1 embodiments of the invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving the central nervous sytem). (The SK-N-MC neuroblastoma cell line is a cell line derived from human brain tissue and is available through the ATCC ™ as cell line number HTB-10). 615 HWHGZ51 Immune Highly preferred indications include immunological disorders such as SUPT CCR4Rag1 gb|AB023888|AB023888gb| described herein under the heading “Immune Activity” and/or “Blood- TNF M29474| Related Disorders” (particularly including, but not limited to, immune HUMRAG1gb| disorders involving T-cells). Highly preferred embodiments of the AJ270944|HSA27094 invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving T-cells). (The SUPT cell line is a human T-cell line). 615 HWHGZ51 Immune Highly preferred indications include immunological disorders such as THP1 c- gb|AF055377|AF055377gb| described herein under the heading “Immune Activity” and/or “Blood- mafCCR7C X84702| Related Disorders” (particularly including, but not limited to, immune XCR3IL5 HSDNABLR2gb| disorders involving monocytes). Highly preferred embodiments of the Z79783|HSCKRL2gb| invention include methods of preventing, detecting, diagnosing, treating X12705| and/or ameliorating disorders of the immune system (particularly HSBCDFIA including, but not limited to, immune disorders involving monocytes). (The THP1 cell line is a human monocyte cell line available through the ATCC ™ as cell line number TIB-202). 615 HWHGZ51 Immune Highly preferred indications include immunological disorders such as U937 CD69ICA gb|Z22576|HSCD69GNAgb| described herein under the heading “Immune Activity” and/or “Blood- MTNF X06990| Related Disorders” (particularly including, but not limited to, immune HSICAM1gb| disorders involving monocytes). Highly preferred embodiments of the AJ270944|HSA27094 invention include methods of preventing, detecting, diagnosing, treating and/or ameliorating disorders of the immune system (particularly including, but not limited to, immune disorders involving monocytes). (The U937 cell line is a human monocyte cell line available through the ATCC ™ as cell line number CRL-1593.2).

Table 2 further characterizes certain encoded polypeptides of the invention, by providing the results of comparisons to protein and protein family databases. The first column provides a unique clone identifier, “Clone ID NO:”, corresponding to a cDNA clone disclosed in Table 1A and/or Table 1B. The second column provides the unique contig identifier, “Contig ID:” which allows correlation with the information in Table 1B. The third column provides the sequence identifier, “SEQ ID NO:”, for the contig polynucleotide sequences. The fourth column provides the analysis method by which the homology/identity disclosed in the Table was determined. The fifth column provides a description of the PFAM/NR hit identified by each analysis. Column six provides the accession number of the PFAM/NR hit disclosed in the fifth column. Column seven, score/percent identity, provides a quality score or the percent identity, of the hit disclosed in column five. Comparisons were made between polypeptides encoded by polynucleotides of the invention and a non-redundant protein database (herein referred to as “NR”), or a database of protein families (herein referred to as “PFAM”), as described below.

The NR database, which comprises the NBRF PIR database, the NCBI GenPept database, and the SIB SwissProt and TrEMBL databases, was made non-redundant using the computer program nrdb2 (Warren Gish, Washington University in Saint Louis). Each of the polynucleotides shown in Table 1B, column 3 (e.g., SEQ ID NO:X or the ‘Query’ sequence) was used to search against the NR database. The computer program BLASTX was used to compare a 6-frame translation of the Query sequence to the NR database (for information about the BLASTX algorithm please see Altshul et al., J. Mol. Biol. 215:403-410 (1990), and Gish and States, Nat. Genet. 3:266-272 (1993). A description of the sequence that is most similar to the Query sequence (the highest scoring ‘Subject’) is shown in column five of Table 2 and the database accession number for that sequence is provided in column six. The highest scoring ‘Subject’ is reported in Table 2 if (a) the estimated probability that the match occurred by chance alone is less than 1.0e-07, and (b) the match was not to a known repetitive element. BLASTX returns alignments of short polypeptide segments of the Query and Subject sequences which share a high degree of similarity; these segments are known as High-Scoring Segment Pairs or HSPs. Table 2 reports the degree of similarity between the Query and the Subject for each HSP as a percent identity in Column 7. The percent identity is determined by dividing the number of exact matches between the two aligned sequences in the HSP, dividing by the number of Query amino acids in the HSP and multiplying by 100. The polynucleotides of SEQ ID NO:X which encode the polypeptide sequence that generates an HSP are delineated by columns 8 and 9 of Table 2.

The PFAM database, PFAM version 2.1, (Sonnhammer, Nucl. Acids Res., 26:320-322, 1998)) consists of a series of multiple sequence alignments; one alignment for each protein family. Each multiple sequence alignment is converted into a probability model called a Hidden Markov Model, or HMM, that represents the position-specific variation among the sequences that make up the multiple sequence alignment (see, e.g., Durbin, et al., Biological sequence analysis: probabilistic models of proteins and nucleic acids, Cambridge University Press, 1998 for the theory of HMMs). The program HMMER version 1.8 (Sean Eddy, Washington University in Saint Louis) was used to compare the predicted protein sequence for each Query sequence (SEQ ID NO:Y in Table 1B.1) to each of the HMMs derived from PFAM version 2.1. A HMM derived from PFAM version 2.1 was said to be a significant match to a polypeptide of the invention if the score returned by HMMER 1.8 was greater than 0.8 times the HMMER 1.8 score obtained with the most distantly related known member of that protein family. The description of the PFAM family which shares a significant match with a polypeptide of the invention is listed in column 5 of Table 2, and the database accession number of the PFAM hit is provided in column 6. Column 7 provides the score returned by HMMER version 1.8 for the alignment. Columns 8 and 9 delineate the polynucleotides of SEQ ID NO:X which encode the polypeptide sequence which show a significant match to a PFAM protein family.

As mentioned, columns 8 and 9 in Table 2, “NT From” and “NT To”, delineate the polynucleotides of “SEQ ID NO:X” that encode a polypeptide having a significant match to the PFAM/NR database as disclosed in the fifth column. In one embodiment, the invention provides a protein comprising, or alternatively consisting of, a polypeptide encoded by the polynucleotides of SEQ ID NO:X delineated in columns 8 and 9 of Table 2. Also provided are polynucleotides encoding such proteins, and the complementary strand thereto.

The nucleotide sequence SEQ ID NO:X and the translated SEQ ID NO:Y are sufficiently accurate and otherwise suitable for a variety of uses well known in the art and described further below. For instance, the nucleotide sequences of SEQ ID NO:X are useful for designing nucleic acid hybridization probes that will detect nucleic acid sequences contained in SEQ ID NO:X or the cDNA contained in ATCC™ Deposit No:Z. These probes will also hybridize to nucleic acid molecules in biological samples, thereby enabling immediate applications in chromosome mapping, linkage analysis, tissue identification and/or typing, and a variety of forensic and diagnostic methods of the invention. Similarly, polypeptides identified from SEQ ID NO:Y may be used to generate antibodies which bind specifically to these polypeptides, or fragments thereof, and/or to the polypeptides encoded by the cDNA clones identified in, for example, Table 1A and/or 1B.

Nevertheless, DNA sequences generated by sequencing reactions can contain sequencing errors. The errors exist as misidentified nucleotides, or as insertions or deletions of nucleotides in the generated DNA sequence. The erroneously inserted or deleted nucleotides cause frame shifts in the reading frames of the predicted amino acid sequence. In these cases, the predicted amino acid sequence diverges from the actual amino acid sequence, even though the generated DNA sequence may be greater than 99.9% identical to the actual DNA sequence (for example, one base insertion or deletion in an open reading frame of over 1000 bases).

Accordingly, for those applications requiring precision in the nucleotide sequence or the amino acid sequence, the present invention provides not only the generated nucleotide sequence identified as SEQ ID NO:X, and a predicted translated amino acid sequence identified as SEQ ID NO:Y, but also a sample of plasmid DNA containing cDNA ATCC™ Deposit No:Z (e.g., as set forth in columns 2 and 3 of Table 1A and/or as set forth, for example, in Table 1B, 6, and 7). The nucleotide sequence of each deposited clone can readily be determined by sequencing the deposited clone in accordance with known methods. Further, techniques known in the art can be used to verify the nucleotide sequences of SEQ ID NO:X. The predicted amino acid sequence can then be verified from such deposits. Moreover, the amino acid sequence of the protein encoded by a particular clone can also be directly determined by peptide sequencing or by expressing the protein in a suitable host cell containing the deposited human cDNA, collecting the protein, and determining its sequence. TABLE 2 cDNA Clone ID Contig ID: SEQ ID NO: X Analysis Method PFam/NR Description PFam/NR Accession Number Score/Percent Identity NT From NT To H2CBG48 745365 11 WUblastx.64 (AAM07193) Cell surface protein. AAM07193 35% 33% 46519 557306 H6EAB28 1352227 13 WUblastx.64 (Q99LL3) CHONDROITIN 4- Q99LL3 68% 89% 115411 3961355 SULFOTRANSFERASE 2. H6EAB28 589947 632 WUblastx.64 (Q9NXY7) CHONDROITIN 4-O- Q9NXY7 85% 98% 112311941 120613521 SULFOTRANSFERASE 82% 16 132 (CHONDROITIN 4-O- SULFOTRANS HACBD91 637482 16 WUblastx.64 NADH dehydrogenase (ubiquinone) pir|JE0383|JE0383 100% 95% 2111306 3571368 (EC 1.6.5.3) chain NDUFB4 - human HACCI17 891114 17 HMMER PFAM: PMP- PF00822 142.7 470 1003 2.1.1 22/EMP/MP20/Claudin family WUblastx.64 (Q8WUW3) Hypothetical 27.7 kDa Q8WUW3 100% 317 1114 protein (Fragment). HACCI17 731877 633 HMMER PFAM: PMP- PF00822 35.6 144 329 2.1.1 22/EMP/MP20/Claudin family WUblastx.64 (Q8WUW3) Hypothetical 27.7 kDa Q8WUW3 80% 57% 244541665 329495962 protein (Fragment). 90% 30% 35311 96786619 75% 100% HADAO89 570689 18 WUblastx.64 (Q9P147) PRO2822. Q9P147 72% 1100 885 HAGAI85 381942 19 WUblastx.64 (O15432) PROBABLE LOW- COP2_HUMAN 100% 96% 91228 234518 AFFINITY COPPER UPTAKE PROTEIN 2 (HCT HAGAN21 1026956 21 WUblastx.64 (Q96NR6) CDNA FLJ30278 fis, Q96NR6 44% 527 835 clone BRACE2002755. HAGAN21 902025 637 WUblastx.64 hypothetical protein pir|T08762|T08762 57% 100% 549283 472167 DKFZp586P2219.1 - human (fragment) HAGBZ81 456414 22 WUblastx.64 (Q9H291) JUNCTATE. Q9H291 85% 77% 18326 329199 HAGDG59 534165 23 HMMER PFAM: short chain dehydrogenase PF00106 182.2 232 795 2.1.1 WUblastx.64 (Q9UKU4) RETINAL SHORT- Q9UKU4 100% 124 1023 CHAIN DEHYDROGENASE/REDUCTASE RETSDR2. HAGFY16 778820 27 WUblastx.64 (Q9BT67) UNKNOWN (PROTEIN Q9BT67 100% 72% 183229338 221402844 FOR MGC: 10924). 100% HAGFY16 381964 638 WUblastx.64 (Q9BT67) UNKNOWN (PROTEIN Q9BT67 86% 99% 60106 104720 FOR MGC: 10924). HAHDB16 635412 28 WUblastx.64 (Q9GMK2) HYPOTHETICAL 10.0 KDA Q9GMK2 75% 69% 641762 522634 PROTEIN. HAHDR32 635357 29 WUblastx.64 (Q9HBU9) POPEYE PROTEIN 2. Q9HBU9 84% 77 811 HAIBP89 727543 31 WUblastx.64 (Q96G79) Similar to RIKEN cDNA Q96G79 99% 290 1261 2610030J16 gene. HAICP19 422672 32 WUblastx.64 (Q9H173) SIL1 PROTEIN Q9H173 100% 83 1465 PRECURSOR. HAJBR69 638516 35 WUblastx.64 (Q9JIG5) UBIQUITIN SPECIFIC Q9JIG5 69% 677 48 PROTEASE (FRAGMENT). HAJBZ75 618530 36 WUblastx.64 hypothetical protein pir|T08708|T08708 99% 25 1869 DKFZp564D116.1 - human (fragment) HAMGG68 731859 38 WUblastx.64 (Q9NX85) CDNA FLJ20378 FIS, Q9NX85 71% 44% 57% 984145414 859140114 CLONE KAIA0536. 70% 56% 571458726 161429658 64% 857 636 HANGG89 852533 640 WUblastx.64 (AAH00634) Reticulon 3. AAH00634 99% 59 418 HANGG89 844216 641 WUblastx.64 (AAH08720) Unknown (protein for AAH08720 83% 51% 70490 10171068 MGC: 8447). HANGG89 692291 642 WUblastx.64 (AAH08720) Unknown (protein for AAH08720 99% 40% 7570 1310198 MGC: 8447). HAPBS03 656755 40 WUblastx.64 (Q99KG1) SIMILAR TO Q99KG1 51% 85% 62% 59593643 175655777 HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN R (FRAGME HAPPW30 1352278 43 WUblastx.64 (Q8WUJ1) Hypothetical 28.7 kDa Q8WUJ1 100% 59 850 protein. HAPPW30 684272 643 WUblastx.64 (Q8WUJ1) Hypothetical 28.7 kDa Q8WUJ1 100% 36% 54982266 2631056844 protein. 100% HAPQT22 587601 44 WUblastx.64 (Q9H728) CDNA: FLJ21463 FIS, Q9H728 53% 69% 634606 590439 CLONE COL04765. HAPUC89 834358 45 WUblastx.64 (Q9BUM1) UNKNOWN Q9BUM1 99% 109 804 (PROTEIN FOR IMAGE: 3050476) (FRAGMENT). HASAV70 1300782 46 WUblastx.64 (Q9NY08) 19A PROTEIN. Q9NY08 82% 7 423 HASAV70 381953 644 WUblastx.64 (Q9NY08) 19A PROTEIN. Q9NY08 100% 4 432 HATAC53 1352276 48 WUblastx.64 (Q8WUN9) Hypothetical 29.4 kDa Q8WUN9 99% 64 840 protein (Fragment). HATAC53 667830 645 WUblastx.64 (Q8WUN9) Hypothetical 29.4 kDa Q8WUN9 98% 66% 66516 593665 protein (Fragment). HATBR65 635514 49 WUblastx.64 (Q96NR6) CDNA FLJ30278 fis, Q96NR6 42% 64% 750617 806751 clone BRACE2002755. HATCP77 748244 51 WUblastx.64 (Q9Y691) MAXIK CHANNEL Q9Y691 100% 10 582 BETA 2 SUBUNIT (LARGE CONDUCTANCE CALCIUM- ACTI HBAFJ33 625916 53 WUblastx.64 (Q9GZR7) HYPOTHETICAL 96.3 KDA Q9GZR7 96% 672 950 PROTEIN (ATP- DEPENDENT RNA HELICASE) ( HBAFV19 843036 54 WUblastx.64 (Q9H068) HYPOTHETICAL 69.9 KDA Q9H068 100% 3 779 PROTEIN. HBCPB32 1352403 56 WUblastx.64 (Q96EP9) Unknown (protein for Q96EP9 92% 100% 6801 844690 IMAGE: 3502817) (Fragment). HBCPB32 1045580 646 HMMER PFAM: Sodium Bile acid symporter PF01758 41.2 87 −230 2.1.1 family WUblastx.64 (Q96EP9) Unknown (protein for Q96EP9 100% 2 589 IMAGE: 3502817) (Fragment). HBCQL32 1027748 647 WUblastx.64 (AAH08044) Unknown (protein for AAH08044 100% 102 182 MGC: 16063). HBGNU56 1352412 58 WUblastx.64 (Q96DB9) FXYD domain- FXY5_HUMAN 100% 125 637 containing ion transport regulator 5 p HBGNU56 1094642 648 HMMER PFAM: ATP1G1/PLM/MAT8 PF02038 70.5 475 609 2.1.1 family WUblastx.64 (Q96DB9) FXYD domain- FXY5_HUMAN 100% 79 612 containing ion transport regulator 5 p HBGNU56 1050255 649 HMMER PFAM: ATP1G1/PLM/MAT8 PF02038 70.5 521 655 2.1.1 family WUblastx.64 (Q96DB9) FXYD domain- FXY5_HUMAN 100% 125 658 containing ion transport regulator 5 p HBHMA23 848016 60 WUblastx.64 (AAM00283) Von Ebner minor AAM00283 100% 99% 64371 1035649 protein. HBHMA23 699815 650 WUblastx.64 (AAM00283) Von Ebner minor AAM00283 100% 92% 709076412 273103291 protein. 97% 94% 61 6647 HBIMB51 963208 61 WUblastx.64 (Q969E3) Urocortin III Q969E3 99% 98 535 (Stresscopin). HBIMB51 672711 651 WUblastx.64 (Q924A4) Urocortin III. Q924A4 61% 64% 29693 517302 HBINS58 1352386 62 WUblastx.64 (Q9D6W7) 2310047N01RIK Q9D6W7 81% 57 578 PROTEIN. HBINS58 961712 652 WUblastx.64 (Q9D6W7) 2310047N01RIK Q9D6W7 80% 71 589 PROTEIN. HBINS58 892924 653 WUblastx.64 (Q9D6W7) 2310047N01RIK Q9D6W7 79% 100 579 PROTEIN. HBJFU48 460392 63 WUblastx.64 (Q9P195) PRO1722. Q9P195 63% 73% 64% 716819667 660718533 HBJLF01 732111 66 HMMER PFAM: Transmembrane 4 family PF00335 131.8 223 891 2.1.1 WUblastx.64 (AAH24685) Similar to AAH24685 93% 133 948 transmembrane 4 superfamily m HBJNC59 1125802 68 WUblastx.64 complement subcomponent C1q pir|S14350|C1HUQA 100% 66 800 chain A precursor [validated] - human HBJNC59 899397 654 HMMER PFAM: Collagen triple helix repeat PF01391 30.1 144 245 2.1.1 (20 copies) WUblastx.64 (Q9H2L7) DC33. Q9H2L7 79% 77 907 HBJNC59 902207 655 HMMER PFAM: C1q domain PF00386 250.2 409 786 2.1.1 WUblastx.64 complement subcomponent C1q pir|S14350|C1HUQA 100% 64 798 chain A precursor [validated] - human HBOEG11 1300752 71 WUblastx.64 (O76076) CONNECTIVE TISSUE O76076 75% 57 806 GROWTH FACTOR-LIKE PROTEIN PRECURSOR (BA44 HBOEG11 1121709 656 HMMER PFAM: Insulin-like growth factor PF00219 45.4 128 340 2.1.1 binding proteins WUblastx.64 (O76076) CONNECTIVE TISSUE O76076 100% 53 802 GROWTH FACTOR-LIKE PROTEIN PRECURSOR (BA44 HBOEG11 1049830 657 HMMER PFAM: Insulin-like growth factor PF00219 45.4 122 334 2.1.1 binding proteins WUblastx.64 (O76076) CONNECTIVE TISSUE O76076 100% 47 796 GROWTH FACTOR-LIKE PROTEIN PRECURSOR (BA44 HBOEG69 793786 72 WUblastx.64 (Q9NS11) Q9NS11 71% 100% 424345 314196 LIPOPOLYSACCHARIDE SPECIFIC RESPONSE-68 PROTEIN. HBXFL29 842802 73 WUblastx.64 (Q8WYF7) POB1. Q8WYF7 99% 4 1008 HCACU58 625923 74 WUblastx.64 (Q9NX85) CDNA FLJ20378 FIS, Q9NX85 69% 548 820 CLONE KAIA0536. HCACV51 1306706 75 WUblastx.64 (Q99LM9) UNKNOWN (PROTEIN Q99LM9 85% 8 1009 FOR MGC: 8251). HCACV51 598022 658 WUblastx.64 (Q96BN2) Similar to RIKEN cDNA Q96BN2 97% 91% 13323 3121015 2900026B15 gene. HCE1Q89 520329 77 WUblastx.64 (Q9NX85) CDNA FLJ20378 FIS, Q9NX85 86% 61% 65% 590645859 525592683 CLONE KAIA0536. HCE2F54 634016 78 HMMER PFAM: Histone-like transcription PF00808 19 868 1005 2.1.1 factor (CBF/NF-Y) and archaeal histone WUblastx.64 (AAH07642) Unknown (protein for AAH07642 82% 298 1122 IMAGE: 3534358) (Fra HCEFB80 1143407 79 WUblastx.64 (Q96FR3) Unknown (protein for Q96FR3 100% 1785 1979 MGC: 18083). HCEFB80 1046853 659 WUblastx.64 (Q96FR3) Unknown (protein for Q96FR3 100% 1777 1971 MGC: 18083). HCEGR33 425212 80 WUblastx.64 (Q9H743) CDNA: FLJ21394 FIS, Q9H743 51% 42% 58% 100213799 107914929 CLONE COL03536. 07 93 HCEMP62 684780 81 WUblastx.64 (Q8WZ37) Hypothetical 43.7 kDa Q8WZ37 75% 78% 41% 484881870 897459183 protein. 94% 926 HCEWE17 941941 83 WUblastx.64 (Q9H310) RH TYPE B Q9H310 95% 100% 9425444 341463566 GLYCOPROTEIN. 92% HCEWE17 893535 661 WUblastx.64 (Q9H310) RH TYPE B Q9H310 78% 75% 100% 4676956763 580730714 GLYCOPROTEIN. 100% 482 HCEWE17 460407 662 WUblastx.64 (Q9H310) RH TYPE B Q9H310 96% 7 105 GLYCOPROTEIN. HCEWE20 543370 84 WUblastx.64 (Q9P1J1) PRO1546. Q9P1J1 76% 79% 501601 551717 HCFOM18 553582 88 WUblastx.64 (Q9H728) CDNA: FLJ21463 FIS, Q9H728 60% 621 490 CLONE COL04765. HCHNF25 1352270 89 WUblastx.64 (AAL76113) Androgen-induced AAL76113 99% 64% 24% 306933716 218828114 basic leucine zipper. 22 25 HCHNF25 658672 663 WUblastx.64 (AAH00499) Jumping translocation AAH00499 91% 180 620 breakpoint. HCNSM70 637547 95 HMMER PFAM: Immunoglobulin domain PF00047 32 224 481 2.1.1 WUblastx.64 (O60487) EPITHELIAL V-LIKE O60487 98% 107 751 ANTIGEN PRECURSOR (EPITHELIAL V-LIKE ANTIG HCNSM70 589445 665 WUblastx.64 (O60487) EPITHELIAL V-LIKE O60487 100% 99% 161408 409806 ANTIGEN PRECURSOR (EPITHELIAL V-LIKE ANTIG HCOOS80 1134974 96 WUblastx.64 (O14641) SEGMENT POLARITY DVL2_HUMAN 100% 8 637 PROTEIN DISHEVELLED HOMOLOG DVL-2 HCOOS80 1045182 666 WUblastx.64 (O14641) SEGMENT POLARITY DVL2_HUMAN 100% 21 683 PROTEIN DISHEVELLED HOMOLOG DVL-2 HCOOS80 1045183 667 WUblastx.64 (O14641) SEGMENT POLARITY DVL2_HUMAN 94% 91% 651 11569 PROTEIN DISHEVELLED HOMOLOG DVL-2 HCUCK44 720291 98 WUblastx.64 hypothetical protein pir|T34520|T34520 97% 21 524 DKFZp564J157.1 - human (fragment) HCUEO60 499242 99 WUblastx.64 (Q96MM0) CDNA FLJ32172 fis, Q96MM0 79% 72% 10431222 9721028 clone PLACE6000555. HCUHK65 651313 100 WUblastx.64 (Q9H3W5) HYPOTHETICAL 79.4 KDA Q9H3W5 100% 11 316 PROTEIN. HCUHK65 880178 668 HMMER PFAM: Leucine Rich Repeat PF00560 92.1 1190 1261 2.1.1 WUblastx.64 (Q9H3W5) HYPOTHETICAL 79.4 KDA Q9H3W5 100% 770 2893 PROTEIN. HCWEB58 1352416 102 WUblastx.64 (Q92WW6) Putative sensor histidine Q92WW6 41% 45% 38% 264166301 3352311167 kinase protein. HCWEB58 1115089 669 HMMER PFAM: Domain found in bacterial PF00672 40.4 442 651 2.1.1 signal proteins WUblastx.64 sensor histidine kinase [imported] - pir|A87396|A87396 36% 31% 379268 915363 Caulobacter crescentus HCWEB58 889268 670 HMMER PFAM: Domain found in bacterial PF00672 41.6 350 559 2.1.1 signal proteins WUblastx.64 sensor histidine kinase [imported] - pir|A87396|A87396 36% 31% 287176 823271 Caulobacter crescentus HCWGU37 1042325 103 WUblastx.64 (O60448) NEURONAL THREAD O60448 43% 75% 63% 272423732 237123262 PROTEIN AD7C-NTP. 65% 7762758 4472579 HCWKC15 553621 104 WUblastx.64 (Q9NX85) CDNA FLJ20378 FIS, Q9NX85 77% 56% 63% 538710708 419663532 CLONE KAIA0536. HCWUM50 639037 106 WUblastx.64 (Q9NWD1) HYPOTHETICAL 61.6 KDA Q9NWD1 94% 73% 21103 1751303 PROTEIN. HCYBG92 598019 107 WUblastx.64 (Q9UPI3) HYPOTHETICAL 57.2 KDA Q9UPI3 100% 76 939 PROTEIN. HDABR72 1301517 108 WUblastx.64 (Q9BTK4) UNKNOWN (PROTEIN Q9BTK4 100% 695 886 FOR MGC: 4663). HDABR72 748225 672 HMMER PFAM: Cytochrome P450 PF00067 21.7 145 282 2.1.1 WUblastx.64 (Q9BTK4) UNKNOWN (PROTEIN Q9BTK4 100% 690 881 FOR MGC: 4663). HDHEB60 499233 109 WUblastx.64 (Q9Y5Y5) PEROXISOMAL Q9Y5Y5 81% 277 1284 BIOGENESIS FACTOR 16. HDHIA94 765171 110 HMMER PFAM: Sodium/calcium exchanger PF01699 121.4 178 615 2.1.1 protein WUblastx.64 (Q9HC58) SODIUM/CALCIUM Q9HC58 90% 10 657 EXCHANGER NCKX3. HDHIA94 637576 673 HMMER PFAM: Sodium/calcium exchanger PF01699 22.9 187 273 2.1.1 protein HDHMA72 547772 111 WUblastx.64 (Q8WVP7) Hypothetical 55.1 kDa Q8WVP7 28% 95% 50% 370076110 389111681 protein. 99% 192 231592 HDLAC10 692299 112 WUblastx.64 (Q9UBJ4) TRANSPOSASE-LIKE Q9UBJ4 99% 29 1378 PROTEIN. HDPBI32 1352360 114 WUblastx.64 (O88407) NEURAL MEMBRANE O88407 92% 37 984 PROTEIN 35. HDPBI32 862851 674 WUblastx.64 (O88407) NEURAL MEMBRANE O88407 95% 89% 599103 1051603 PROTEIN 35. HDPBI32 590733 675 HMMER PFAM: Uncharacterized protein PF01027 126.8 51 461 2.1.1 family HDPBQ71 1160316 115 WUblastx.64 (Q9BRE2) HYPOTHETICAL 68.4 KDA Q9BRE2 100% 90 1928 PROTEIN (FRAGMENT). HDPBQ71 727200 676 WUblastx.64 (Q9BRE2) HYPOTHETICAL 68.4 KDA Q9BRE2 99% 21 1859 PROTEIN (FRAGMENT). HDPBQ71 886067 677 WUblastx.64 (Q9H2V9) CDA08. Q9H2V9 100% 65% 153216918 199926432 44% 21% 93% 21456186 215511541 HDPCJ91 740748 116 WUblastx.64 (Q9H387) PRO2550. Q9H387 53% 56% 23692377 24072676 HDPCY37 837699 118 HMMER PFAM: Glycosyl hydrolase family PF01532 627.5 199 1521 2.1.1 47 WUblastx.64 (Q9H886) CDNA FLJ13869 FIS, Q9H886 99% 76 1809 CLONE THYRO1001287, WEAKLY SIMILAR TO MAN HDPCY37 604114 678 HMMER PFAM: Glycosyl hydrolase family PF01532 324 199 834 2.1.1 47 WUblastx.64 (Q9H886) CDNA FLJ13869 FIS, Q9H886 97% 99% 76813 8401808 CLONE THYRO1001287, WEAKLY SIMILAR TO MAN HDPFB02 898208 119 WUblastx.64 (Q9BXR1) COSTIMULATORY Q9BXR1 98% 97% 97% 146877495 499174962 MOLECULE. 76% 568 0900 HDPFB02 1056541 679 HMMER PFAM: Immunoglobulin domain PF00047 53.2 610 804 2.1.1 WUblastx.64 (Q9BXR1) COSTIMULATORY Q9BXR1 99% 139 1086 MOLECULE. HDPFB02 997408 680 HMMER PFAM: Immunoglobulin domain PF00047 26.9 305 562 2.1.1 WUblastx.64 (Q9HD18) TRANSMEMBRANE Q9HD18 99% 218 1123 PROTEIN B7-H2 ICOS LIGAND (B7-RELATED PROTEIN- HDPFF39 588697 120 WUblastx.64 (O96005) CLEFT LIP AND O96005 100% 100% 397 29762 PALATE TRANSMEMBRANE PROTEIN 1. HDPGP94 823355 123 WUblastx.64 (Q14288) HYPOTHETICAL Q14288 47% 88% 48% 614129790 216127170 PROTEIN (FRAGMENT). 28% 39% 917671093 015378901 35% 27% 12752282 0902082 HDPJF37 704487 125 WUblastx.64 (Q9BSQ8) UNKNOWN (PROTEIN Q9BSQ8 94% 36% 93% 10515819 650718153 FOR IMAGE: 3510191) (FRAGMENT). HDPMM88 972734 126 HMMER PFAM: E1-E2 ATPase PF00122 31 475 543 2.1.1 WUblastx.64 (P98198) POTENTIAL AT1D_HUMAN 68% 32% 1062917 29072991 PHOSPHOLIPID- TRANSPORTING ATPASE ID (EC HDPMM88 906121 681 WUblastx.64 (Q96NQ7) CDNA FLJ30324 fis, Q96NQ7 50% 76% 3563 403365 clone BRACE2007138, weakly similar to PRO HDPMM88 902299 682 WUblastx.64 (P98199) POTENTIAL AT1D_MOUSE 73% 2 172 PHOSPHOLIPID- TRANSPORTING ATPASE ID (EC HDPMM88 885059 683 WUblastx.64 (AAH07837) Unknown (protein for AAH07837 75% 69% 63598 1662 IMAGE: 4111596) (Fra HDPMM88 874074 684 WUblastx.64 (P98198) POTENTIAL AT1D_HUMAN 65% 1023 1 PHOSPHOLIPID- TRANSPORTING ATPASE ID (EC HDPNC61 637585 127 WUblastx.64 (Q8WY51) HC6. Q8WY51 52% 64% 65437 82778 HDPND46 637586 128 WUblastx.64 (Q9BR26) DJ257E24.3 (NOVEL Q9BR26 81% 12 1466 PROTEIN) (FRAGMENT). HDPOE32 897276 129 WUblastx.64 (Q9BW48) MY047 PROTEIN. Q9BW48 98% 64 345 HDPOH06 683371 130 HMMER PFAM: Uncharacterized membrane PF01554 90.8 255 596 2.1.1 protein family WUblastx.64 (Q96FL8) Hypothetical 61.9 kDa Q96FL8 99% 18 977 protein. HDPOZ56 1352319 131 WUblastx.64 (BAB84923) FLJ00168 protein BAB84923 100% 28 1791 (Fragment). HDPOZ56 815653 687 HMMER PFAM: Flavin containing amine PF01593 431.1 307 1614 2.1.1 oxidase WUblastx.64 (BAB84923) FLJ00168 protein BAB84923 99% 40 1800 (Fragment). HDPOZ56 743479 688 HMMER PFAM: Flavin containing amine PF01593 185.2 200 949 2.1.1 oxidase WUblastx.64 (BAB84923) FLJ00168 protein BAB84923 98% 99% 100% 1979522 9581647202 (Fragment). HDPSP54 744440 132 WUblastx.64 (BAB85063) CDNA FLJ23790 fis, BAB85063 99% 2 307 clone HEP21466. HDPTD15 692917 133 WUblastx.64 (Q9BU29) UNKNOWN (PROTEIN Q9BU29 97% 937 833 FOR IMAGE: 3954899) (FRAGMENT). HDPTK41 744824 134 WUblastx.64 (BAB11849) MOP-2. BAB11849 97% 94% 1013102 11261025 HDPUG50 684120 135 WUblastx.64 (Q9BVK2) UNKNOWN (PROTEIN Q9BVK2 96% 55 1599 FOR MGC: 2840). HDPUH26 866433 136 WUblastx.64 (Q8VHE7) Hypothetical 67.5 kDa Q8VHE7 80% 69% 261162 1733290 protein. HDPUW68 812737 137 HMMER PFAM: Immunoglobulin domain PF00047 38.9 844 1005 2.1.1 WUblastx.64 (Q9Y286) QA79 MEMBRANE Q9Y286 100% 40 1440 PROTEIN, ALLELIC VARIANT AIRM-1B PRECURSOR. HDPVH60 796865 138 WUblastx.64 (BAB55096) CDNA FLJ14508 fis, BAB55096 95% 38% 58% 235288244 294473294 clone NT2RM1000421, w 88% 40% 288456121 161052114 29% 31% 513892381 871607294 42% 38% 607798131 186115441 27% 42% 716041613 478201719 24% 30% 160716581 031906203 25% 27% 580162812 220771903 86% 29% 00238 1598294 35% 42% HDPVW11 1036997 139 HMMER PFAM: AMP-binding enzyme PF00501 30.2 913 1344 2.1.1 WUblastx.64 (Q9BTY5) UNKNOWN (PROTEIN Q9BTY5 52% 27% 86% 134410961 199113322 FOR MGC: 4365). 30% 73% 924613 0972001647 HDPVW11 896530 690 WUblastx.64 (Q9BTY5) UNKNOWN (PROTEIN Q9BTY5 84% 2 397 FOR MGC: 4365). HDPWN93 992925 140 WUblastx.64 (AAH25255) Similar to hypothetical AAH25255 99% 45 2450 protein FLJ21347 HDPWN93 887914 691 WUblastx.64 (AAH25255) Similar to hypothetical AAH25255 97% 68% 35619 661714 protein FLJ21347 HDPWN93 905983 692 WUblastx.64 (Q9H747) CDNA: FLJ21347 FIS, Q9H747 68% 99% 27205 1552487 CLONE COL02724. HDPWU34 630354 141 HMMER PFAM: POT family PF00854 77.2 432 857 2.1.1 WUblastx.64 (Q9P2X9) PEPTIDE Q9P2X9 100% 3 1091 TRANSPORTER 3. HDQHD03 1309175 142 WUblastx.64 (AAH25621) Hypothetical 137.4 kDa AAH25621 86% 520 1263 protein (Fragment HDQHD03 834692 694 HMMER PFAM: Cyclic nucleotide-binding PF00027 44.3 709 870 2.1.1 domain WUblastx.64 (AAH25621) Hypothetical 137.4 kDa AAH25621 84% 505 1248 protein (Fragment HDTBD53 972757 143 WUblastx.64 (Q9BTV4) UNKNOWN (PROTEIN Q9BTV4 100% 183 1382 FOR MGC: 3222). HDTBD53 906342 695 WUblastx.64 (Q9BTV4) UNKNOWN (PROTEIN Q9BTV4 99% 187 1386 FOR MGC: 3222). HDTBP04 1307742 144 WUblastx.64 (Q9D5J3) 4930432K09RIK Q9D5J3 38% 70 720 PROTEIN. HDTBP04 543618 696 WUblastx.64 (Q9D5J3) 4930432K09RIK Q9D5J3 38% 65 718 PROTEIN. HDTDQ23 1306984 145 WUblastx.64 calcium-binding protein (clone pir|S04970|S04970 100% 1611 1709 pMP41) - mouse (fragment) HDTDQ23 879009 697 WUblastx.64 calcium-binding protein (clone pir|S04970|S04970 100% 1623 1721 pMP41) - mouse (fragment) HDTDQ23 751707 698 WUblastx.64 calcium-binding protein (clone pir|S04970|S04970 100% 1623 1721 pMP41) - mouse (fragment) HDTFE17 1043391 148 WUblastx.64 (Q9UJU8) JM24 PROTEIN Q9UJU8 100% 84% 14955343 1181089705 (FRAGMENT). 100% HDTFE17 874477 702 WUblastx.64 (Q8WYU2) Hypothetical 44.0 kDa Q8WYU2 100% 45% 8554337 112622612 protein. 72% HDTFE17 892317 703 HMMER PFAM: Transmembrane amino acid PF01490 86.4 116 481 2.1.1 transporter protein WUblastx.64 (Q8WYU2) Hypothetical 44.0 kDa Q8WYU2 100% 97% 45733 672461 protein. HDTIT10 839264 150 HMMER PFAM: Phosphatidylethanolamine- PF01161 50.9 463 621 2.1.1 binding protein WUblastx.64 (Q96DV4) Similar to RIKEN cDNA Q96DV4 100% 82% 819352 911858 4733401F03 gene. HDTIT10 834697 704 WUblastx.64 (Q96DV4) Similar to RIKEN cDNA Q96DV4 98% 343 903 4733401F03 gene. HDTMK50 1011485 151 WUblastx.64 (Q9H728) CDNA: FLJ21463 FIS, Q9H728 64% 72% 11191351 10451121 CLONE COL04765. HE2DY70 722217 152 WUblastx.64 (Q9BS33) SIMILAR TO Q9BS33 100% 9 167 HYPOTHETICAL PROTEIN FLJ11218. HE2FV03 396139 155 WUblastx.64 (Q8WX31) BA382H24.3 (multiple Q8WX31 73% 281 805 PDZ domain protein) (Fragment). HE2NV57 740750 156 WUblastx.64 (Q9UGV6) BK445C9.3 (HIGH- Q9UGV6 31% 66% 32171 866106 MOBILITY GROUP (NONHISTONE CHROMOSOMAL) PROT HE2PD49 638617 157 WUblastx.64 (Q9BSR6) SIMILAR TO RIKEN Q9BSR6 100% 403 849 CDNA 2410018G23 GENE. HE8DS15 847060 160 WUblastx.64 (Q9WVT0) SEVEN Q9WVT0 80% 24% 87% 148269 270146985 TRANSMEMBRANE RECEPTOR. HE8MH91 589450 161 WUblastx.64 (Q9H8Z4) CDNA FLJ13121 FIS, Q9H8Z4 98% 9 410 CLONE NT2RP3002687. HE8QV67 1050076 162 WUblastx.64 (BAB55430) CDNA FLJ14978 fis, BAB55430 100% 31% 321487114 425600201 clone VESEN1000122. 100% 96% 03577800 168472911 96% 98% 08 HE8QV67 1050077 707 WUblastx.64 (BAB55430) CDNA FLJ14978 fis, BAB55430 100% 86% 150031091 198820624 clone VESEN1000122. 30% 30% 99% 366334 614551500 HE9BK23 675382 163 HMMER PFAM: Fibrinogen beta and gamma PF00147 77.2 762 959 2.1.1 chains, C-terminal globular domain WUblastx.64 (Q9Y5C1) ANGIOPOIETIN 5. Q9Y5C1 100% 92% 95839 1419959 HE9DG49 1299935 165 WUblastx.64 (Q9NYL4) FK506 BINDING Q9NYL4 100% 70 672 PROTEIN PRECURSOR. HE9DG49 658678 708 HMMER PFAM: FKBP-type peptidyl-prolyl PF00254 91 211 492 2.1.1 cis-trans isomerases WUblastx.64 (Q9NYL4) FK506 BINDING Q9NYL4 100% 70 672 PROTEIN PRECURSOR. HE9DG49 382000 709 HMMER PFAM: FKBP-type peptidyl-prolyl PF00254 91 −71 −352 2.1.1 cis-trans isomerases WUblastx.64 (Q9NYL4) FK506 BINDING Q9NYL4 100% 86% 57878 679674 PROTEIN PRECURSOR. HE9OW20 1352337 168 WUblastx.64 (CAC41349) Alpha2- CAC41349 95% 129 1151 glucosyltransferase. HE9OW20 838598 710 WUblastx.64 (CAC41349) Alpha2- CAC41349 99% 142 996 glucosyltransferase. HE9OW20 834400 711 WUblastx.64 (CAC41349) Alpha2- CAC41349 93% 95% 129449 4971051 glucosyltransferase. HE9RM63 886167 169 WUblastx.64 (Q9NV86) CDNA FLJ10873 FIS, Q9NV86 40% 94% 199582 20871113 CLONE NT2RP4001730, WEAKLY SIMILAR TO UDP HEAAR07 561524 170 WUblastx.64 probable transposase - human pir|S72481|S72481 57% 89% 75% 691102021 858107633 transposon MER37 78% 33% 0833784332 210158647 55% 03 HEBCM63 484643 173 WUblastx.64 (Q9BYH1) SEZ6L. Q9BYH1 91% 12 449 HEBEJ18 701802 174 WUblastx.64 (AAH00573) HSPC163 protein. AAH00573 100% 51 467 HEEAG23 684254 175 HMMER PFAM: emp24/gp25L/p24 family PF01105 36.2 63 185 2.1.1 WUblastx.64 (AAH23041) Similar to RIKEN AAH23041 100% 99% 114406 185780 cDNA 2400003B06 gene. HEEAJ02 633657 176 WUblastx.64 (Q9BW86) Q9BW86 80% 54 761 PHOSPHATIDYLETHANOLAMINE N-METHYLTRANSFERASE. HEEAQ11 777843 177 HMMER PFAM: Cystatin domain PF00031 39.7 360 638 2.1.1 WUblastx.64 (Q9H4G1) BA218C14.1 (NOVEL Q9H4G1 100% 213 653 CYSTATIN FAMILY MEMBER). HEEBI05 1307611 178 WUblastx.64 (Q9N7S5) PROBABLE Q9N7S5 32% 252 635 PROTEOPHOSPHOGLYCAN (FRAGMENT). HEEBI05 1047700 712 WUblastx.64 (Q9N7S5) PROBABLE Q9N7S5 32% 332 715 PROTEOPHOSPHOGLYCAN (FRAGMENT). HEGAH43 532596 179 WUblastx.64 (Q9H1M5) BA530N10.1 (NOVEL Q9H1M5 100% 29 361 PROTEIN). HEGAN94 885637 180 WUblastx.64 colipase precursor, pancreatic - dog pir|A46717|A46717 36% 148 393 HEGAN94 769649 713 HMMER PFAM: Colipase PF01114 24 229 405 2.1.1 WUblastx.64 colipase precursor, pancreatic - dog pir|A46717|A46717 36% 229 474 HEGBS69 1048170 714 WUblastx.64 (Q9H056) HYPOTHETICAL 12.5 KDA Q9H056 100% 1125 778 PROTEIN. HELGK31 681138 182 HMMER PFAM: DHHC zinc finger domain PF01529 95.1 659 820 2.1.1 WUblastx.64 (Q9NPG8) CDNA FLJ10479 FIS, Q9NPG8 83% 209 1240 CLONE NT2RP2000120 (DC1) (HYPOTHETICAL 39 HELGK31 340352 715 HMMER PFAM: DHHC zinc finger domain PF01529 95.1 −82 −243 2.1.1 WUblastx.64 (Q9NPG8) CDNA FLJ10479 FIS, Q9NPG8 98% 36% 100% 24236498 4961281274 CLONE NT2RP2000120 (DC1) (HYPOTHETICAL 39 HELHD85 847372 183 WUblastx.64 (Q9N083) UNNAMED PORTEIN Q9N083 52% 53% 67% 171516481 165315591 PRODUCT. 881 705 HELHL48 696945 184 HMMER PFAM: DHHC zinc finger domain PF01529 124.3 797 991 2.1.1 WUblastx.64 hypothetical protein pir|T47144|T47144 96% 359 1414 DKFZp761E1347.1 - human (fragment) HELHL48 610025 716 HMMER PFAM: DHHC zinc finger domain PF01529 124.3 199 393 2.1.1 WUblastx.64 hypothetical protein pir|T47144|T47144 100% 98% 47058510 586818471 DKFZp761E1347.1 - human 90% (fragment) HEMAM41 741647 185 WUblastx.64 (Q8VDR1) Similar to RIKEN cDNA Q8VDR1 63% 385 744 2310044D20 gene. HEMAM41 419870 717 WUblastx.64 (Q8VDR1) Similar to RIKEN cDNA Q8VDR1 83% 398 745 2310044D20 gene. HEPAA46 596830 186 WUblastx.64 (Q96PH6) ESC42. Q96PH6 100% 18 386 HESAJ10 526013 190 WUblastx.64 (Q8WWX9) Selenoprotein SelM. Q8WWX9 96% 95% 64% 566405541 841545582 HETAB45 609827 191 WUblastx.64 (Q9NXH2) CDNA FLJ20254 FIS, Q9NXH2 98% 99% 6463 795647 CLONE COLF6926. HETLM70 1177512 193 WUblastx.64 (AAH25323) Similar to hypothetical AAH25323 99% 3 1022 protein FLJ21240 HETLM70 1046327 719 WUblastx.64 (AAH25323) Similar to hypothetical AAH25323 99% 3 1022 protein FLJ21240 HETLM70 1046328 720 WUblastx.64 (AAH25323) Similar to hypothetical AAH25323 98% 100% 1012 25646 protein FLJ21240 HFABG18 847073 194 WUblastx.64 (Q9QZE9) TM6P1. Q9QZE9 95% 88% 53237 253797 HFAMB72 490697 195 WUblastx.64 (Q9Y6F6) JAW1-RELATED Q9Y6F6 94% 69% 6721 722669 PROTEIN MRVI1A LONG ISOFORM. HFCCQ50 579993 197 HMMER PFAM: Galactosyltransferase PF01762 130.8 365 1042 2.1.1 WUblastx.64 (Q9C0J1) BETA-1,3-N- Q9C0J1 95% 35 1102 ACETYLGLUCOSAMINYLTRANSFERASE BGN-T4. HFFAL36 560639 200 WUblastx.64 (O75525) T-STAR. O75525 100% 568 657 HFGAD82 513669 201 WUblastx.64 membrane glycoprotein M6 - mouse pir|I78556|I78556 92% 249 410 HFIIZ70 1043350 202 WUblastx.64 (Q8WWX9) Selenoprotein SelM. Q8WWX9 93% 86% 91% 833244239 919212458 98% 87 1145 HFIIZ70 906708 721 WUblastx.64 (Q8WWX9) Selenoprotein SelM. Q8WWX9 98% 93% 98% 103888474 119697024 91% 474 1509 HFKET18 889515 203 WUblastx.64 (Q9HAD8) CDNA FLJ11786 FIS, Q9HAD8 63% 54% 42% 138412301 148513971 CLONE HEMBA1006036. 66% 50% 444139014 533143415 71 33 HFKFG02 634743 204 WUblastx.64 ISOFORM OAT1.2 OF O95742 tr_vs|O95742- 89% 100% 11253 265564 01|O95742 HFPCX09 1309793 208 WUblastx.64 (O95970) LEUCINE-RICH O95970 100% 161 1831 GLIOMA-INACTIVATED PROTEIN PRECURSOR. HFPCX09 835390 722 HMMER PFAM: Leucine rich repeat C- PF01463 46.3 741 890 2.1.1 terminal domain WUblastx.64 (O95970) LEUCINE-RICH O95970 99% 225 1895 GLIOMA-INACTIVATED PROTEIN PRECURSOR. HFPCX09 598723 723 WUblastx.64 (O95970) LEUCINE-RICH O95970 86% 94% 161169 2981830 GLIOMA-INACTIVATED PROTEIN PRECURSOR. HFPCX36 526635 209 WUblastx.64 (Q96NR6) CDNA FLJ30278 fis, Q96NR6 56% 66% 680450 775680 clone BRACE2002755. HFTCU19 735139 211 WUblastx.64 (Q96B80) Similar to RIKEN cDNA Q96B80 88% 20 802 0610040E02 gene. HFTDL56 695976 212 HMMER PFAM: Neurotransmitter-gated ion- PF00065 769.9 168 1574 2.1.1 channel WUblastx.64 (P04760) ACETYLCHOLINE ACHG_MOUSE 99% 93 1649 RECEPTOR PROTEIN, GAMMA CHAIN PRECUR HFVAB79 1300736 214 WUblastx.64 (Q9BX93) GROUP XIII Q9BX93 100% 133 714 SECRETED PHOSPHOLIPASE A2. HFVAB79 565076 725 WUblastx.64 (Q9BX93) GROUP XIII Q9BX93 100% 139 720 SECRETED PHOSPHOLIPASE A2. HFXGT26 745381 220 WUblastx.64 (O95662) POT. ORF VI O95662 57% 162 689 (FRAGMENT). HFXHK73 609826 223 WUblastx.64 (Q9H960) CDNA FLJ12988 FIS, Q9H960 58% 50% 11641749 10421714 CLONE NT2RP3000080. HFXKJ03 505207 224 WUblastx.64 (O62658) LINE-1 ELEMENT O62658 34% 36% 492920 292525 ORF2. HFXKT05 658690 225 WUblastx.64 (Q9H5H7) CDNA: FLJ23425 FIS, Q9H5H7 81% 5 1015 CLONE HEP22862. HFXKY27 634161 226 WUblastx.64 (Q9P147) PRO2822. Q9P147 86% 70% 812928 768815 HGBFO79 422794 227 WUblastx.64 (AAH06833) Similar to AAH06833 78% 96% 72134 1401147 DKFZP586F1524 protein. HGBIB74 837220 229 WUblastx.64 hypothetical protein ZK858.6 - pir|T28058|T28058 50% 51% 65% 138724827 149443973 Caenorhabditis elegans 62% 23 01403 HGBIB74 838602 727 WUblastx.64 (Q9V3N6) BG: DS00797.1 Q9V3N6 65% 82% 81% 736537125 125774015 PROTEIN. 27% 57% 122361 05537474 HGBIB74 899864 728 WUblastx.64 (Q9V3N6) BG: DS00797.1 Q9V3N6 71% 12 950 PROTEIN. HHAAF20 838603 231 WUblastx.64 (AAH06738) Hypothetical 47.5 kDa AAH06738 85% 81% 540245 728580 protein. HHBCS39 1003028 232 WUblastx.64 (Q9H763) CDNA: FLJ21269 FIS, Q9H763 98% 17 601 CLONE COL01745. HHBCS39 883427 729 WUblastx.64 (Q9H763) CDNA: FLJ21269 FIS, Q9H763 98% 63 647 CLONE COL01745. HHEAA08 638231 233 WUblastx.64 (Q9BVD9) UNKNOWN (PROTEIN Q9BVD9 61% 74% 19232147 18701923 FOR MGC: 5149). HHEMM74 941955 236 WUblastx.64 (Q96QU0) Calcium-promoted Ras Q96QU0 99% 1741 2046 inactivator. HHEMM74 906815 732 WUblastx.64 (Q9HBS7) HYPOTHETICAL 14.2 KDA Q9HBS7 66% 64% 731592 880735 PROTEIN. HHEMM74 902458 733 WUblastx.64 (Q96QU0) Calcium-promoted Ras Q96QU0 99% 89% 458140 1681253 inactivator. HHEMM74 895682 734 WUblastx.64 (Q96QU0) Calcium-promoted Ras Q96QU0 83% 100% 316287 477316 inactivator. HHEPM33 877639 239 WUblastx.64 (Q96BH1) Ring finger protein 25. Q96BH1 97% 100% 101185 12301373 HHEPU04 838217 241 WUblastx.64 (Q9BQB6) UNKNOWN (PROTEIN Q9BQB6 80% 259 747 FOR MGC: 11276) (PROTEIN FOR IMAGE: 3455200). HHEPU04 897457 735 blastx.2 (BC000828) Unknown (protein for gb|AAH00828.1|AAH00828 80% 267 755 IMAGE: 3455200) [Homo sapiens] HHEPU04 535730 736 WUblastx.64 (Q9BQB6) UNKNOWN (PROTEIN Q9BQB6 72% 83% 100% 32621745 424339218 FOR MGC: 11276) (PROTEIN FOR IMAGE: 3455200). HHFBY53 821330 242 WUblastx.64 (Q9LGZ9) GENOMIC DNA, Q9LGZ9 100% 100% 746745744 868867866 CHROMOSOME 3, BAC 100% 100% 745744745 867866867 CLONE: F1D9. 100% 100% 744745744 866867866 100% 745744745 867866867 100% 100% 744745744 866867866 100% 100% 745744745 867866867 100% 100% 744745744 866867866 100% 745744745 867866867 100% 100% 744745744 866867866 100% 100% 745744745 867866867 100% 100% 744745744 866867866 100% 745744745 867866867 100% 100% 744745744 866867866 100% 100% 745744745 867866867 100% 100% 744745744 866867866 100% 745744745 867866867 100% 100% 744745744 866867866 100% 100% 745744745 867866867 100% 100% 744745744 866867866 100% 745744745 867866867 100% 100% 744745744 866867866 100% 100% 745744745 867866867 100% 100% 744745744 866867866 100% 745744745 867866867 100% 100% 744745745 866867867 100% 100% 745744745 867866867 100% 100% 744745744 866867866 100% 745744745 867866867 100% 100% 744745744 866867866 100% 100% 745744745 867866867 100% 100% 744745744 866867866 100% 745744745 867866867 100% 100% 744745744 866867866 100% 100% 745744745 867866867 100% 100% 744745744 866867866 100% 745744745 867866867 100% 100% 744745744 866867866 100% 100% 745744745 867866867 100% 100% 744745744 866867866 100% 745744745 867866867 100% 100% 744745744 866867866 100% 100% 745744745 867866867 100% 100% 744745744 866867866 100% 745744745 867866867 100% 100% 744745744 866867866 100% 100% 745744744 867866866 100% 100% 744745744 866867866 100% 745744745 867866867 100% 100% 744745744 866867866 100% 100% 745744745 867866867 100% 100% 744745744 866867866 100% 745744745 867866867 100% 100% 744745744 866867866 100% 100% 745744745 867866867 100% 100% 744745744 866867866 100% 745744745 867866867 100% 100% 744745744 866867866 100% 100% 745744745 867866867 100% 100% 744745744 866867866 100% 745744745 867866867 100% 100% 744745744 866867866 100% 100% 745744745 867866867 100% 100% 744745744 866867866 100% 745744745 867866867 100% 100% 744745744 866867866 100% 100% 745744745 867866867 100% 100% 744745744 866867866 100% 745744745 867866867 100% 100% 744745744 866867866 100% 100% 745744745 867866867 100% 100% 744745744 866867866 100% 745744745 867866867 100% 100% 744745744 866867866 100% 100% 745744745 867866867 100% 100% 744745744 866867866 100% 745744745 867866867 100% 100% 744745744 866867866 100% 100% 745744745 867866867 100% 100% 744745744 866867866 100% 745744745 867866867 100% 100% 744745744 866867866 100% 100% 745744745 867866867 100% 100% 744745744 866867866 100% 745744745 867866867 100% 100% 744745744 866867866 100% 100% 745744745 867866867 100% 100% 744745744 866867866 100% 745744745 867866867 100% 100% 744744744 866866866 100% 100% 745744745 867866867 100% 100% 744745744 866867866 100% 745744745 867866867 100% 100% 744745744 866867866 100% 100% 745744745 867866867 100% 100% 744745744 866867866 100% 745744745 867866867 100% 100% 744745744 866867866 100% 100% 745744745 867866867 100% 100% 744745744 866867866 100% 745744745 867866867 100% 100% 744745744 866867866 100% 100% 745744745 867866867 100% 100% 744745744 866867866 100% 745744745 867866867 100% 100% 744745744 866867866 100% 100% 745744745 867866867 100% 100% 744745744 866867866 100% 745744745 867866867 100% 100% 744745744 866867866 100% 100% 745744744 867866866 100% 100% 744745744 866867866 100% 745744745 867866867 100% 100% 744745744 866867866 100% 100% 745744745 867866867 100% 100% 744745744 866867866 100% 745744745 867866867 100% 100% 744745744 866867866 100% 100% 745744745 867866867 100% 100% 744745744 866867866 100% 745744745 867866867 100% 100% 744745745 866867867 100% 100% 745744745 867866867 100% 100% 744745744 866867866 100% 745744745 867866867 100% 100% 744745744 866867866 100% 100% 745744745 867866867 100% 100% 745745744 867867866 100% 745744745 867866867 100% 100% 744745745 866867867 100% 100% 745744744 867866866 100% 100% 744745744 866867866 100% 724 867 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 95% 95% 89% HHFEC49 905849 243 WUblastx.64 (Q9D1N2) 1110002J19RIK Q9D1N2 55% 30 500 PROTEIN. HHFFJ48 634521 244 WUblastx.64 (Q9CWA7) 0610010F05RIK Q9CWA7 49% 1362 1598 PROTEIN (FRAGMENT). HHFGR93 865581 245 WUblastx.64 (Q96AP7) Hypothetical 41.2 kDa Q96AP7 100% 132 1301 protein. HHFGR93 691402 737 HMMER PFAM: Immunoglobulin domain PF00047 36.3 628 807 2.1.1 WUblastx.64 (Q96AP7) Hypothetical 41.2 kDa Q96AP7 98% 99% 819130 1298828 protein. HHFHR32 411470 247 WUblastx.64 (Q99LX9) SIMILAR TO SINGLE- Q99LX9 100% 1 762 STRANDED-DNA-BINDING PROTEIN. HHFOJ29 1127491 248 WUblastx.64 (Q9H7P4) FLJ00024 PROTEIN Q9H7P4 99% 592 65 (FRAGMENT). HHFOJ29 1040264 738 WUblastx.64 (Q9H7P4) FLJ00024 PROTEIN Q9H7P4 99% 268 789 (FRAGMENT). HHFOJ29 1042456 739 WUblastx.64 (Q9H7P4) FLJ00024 PROTEIN Q9H7P4 61% 90% 81196 4101 (FRAGMENT). HHGBO91 520198 249 WUblastx.64 (Q96NR6) CDNA FLJ30278 fis, Q96NR6 86% 66% 46% 622531439 687620353 clone BRACE2002755. 46% 633 496 HHGCM76 662329 250 WUblastx.64 (Q96FV2) Unknown (protein for Q96FV2 94% 98% 7378 114536 IMAGE: 3945715) (Fragment). HHGCM76 383547 740 WUblastx.64 (Q96FV2) Unknown (protein for Q96FV2 94% 98% 7378 114536 IMAGE: 3945715) (Fragment). HHGDW43 554613 253 WUblastx.64 (Q9P1J1) PRO1546. Q9P1J1 59% 52% 707774 787887 HHPGO40 1299927 255 WUblastx.64 (Q9HBW1) Brain tumor associated Q9HBW1 74% 30% 191338 976928 protein NAG14. HHPGO40 753270 741 HMMER PFAM: Leucine Rich Repeat PF00560 122 542 613 2.1.1 WUblastx.64 (Q9HBW1) Brain tumor associated Q9HBW1 74% 30% 191338 967928 protein NAG14. HHPGO40 560969 742 HMMER PFAM: Leucine Rich Repeat PF00560 77 548 619 2.1.1 WUblastx.64 (Q9HBW1) Brain tumor associated Q9HBW1 71% 31% 74% 739691197 984933754 protein NAG14. HILCF66 636025 258 WUblastx.64 (Q9CWZ1) 2400006A19RIK Q9CWZ1 100% 96% 14351243 15301323 PROTEIN. HJACG02 1307789 259 WUblastx.64 (Q9HD89) CYSTEINE-RICH Q9HD89 100% 66 389 SECRETED PROTEIN (C/EBP- EPSILON REGULATED MYEL HJACG02 509948 743 WUblastx.64 (Q9HD89) CYSTEINE-RICH Q9HD89 100% 47 370 SECRETED PROTEIN (C/EBP- EPSILON REGULATED MYEL HJACG30 895505 260 WUblastx.64 (Q9UM21) UDP-GLCNAC: A-1,3- Q9UM21 96% 291 389 D-MANNOSIDE B-1,4-N- ACETYLGLUCOSAMINYLTRANS HJACG30 774300 745 WUblastx.64 (Q9D399) 6330415B21RIK Q9D399 80% 220 297 PROTEIN. HJBCU04 877643 261 WUblastx.64 (Q9Y3P8) SIT PROTEIN Q9Y3P8 100% 36 623 PRECURSOR. HJBCY35 719729 262 WUblastx.64 hypothetical protein pir|T08758|T08758 100% 1 1212 DKFZp586J0619.1 - human (fragment) HJMBM38 545752 264 WUblastx.64 (Q9CS66) 5730496N17RIK Q9CS66 83% 3 722 PROTEIN (FRAGMENT). HJPAD75 651337 267 WUblastx.64 (Q9H5F8) CDNA: FLJ23476 FIS, Q9H5F8 98% 8 232 CLONE HSI14935. HJPCP42 852573 747 WUblastx.64 (Q9VL06) CG5604 PROTEIN. Q9VL06 54% 19 315 HJPCP42 824612 748 WUblastx.64 cut1 protein - fission yeast pir|A35694|A35694 42% 7 201 (Schizosaccharomyces pombe) HKAAE44 564406 269 WUblastx.64 (Q969S6) Unknown (protein for Q969S6 86% 113 520 MGC: 15961) (protein for MGC: 14327). HKAAH36 1352332 270 WUblastx.64 (AAH08036) Kallikrein 5. AAH08036 100% 128 1006 HKAAH36 1352331 749 WUblastx.64 (AAH08036) Kallikrein 5. AAH08036 71% 295 846 HKAAH36 1352330 750 WUblastx.64 (AAH08036) Kallikrein 5. AAH08036 100% 182 1060 HKAAH36 836040 751 WUblastx.64 (AAH08036) Kallikrein 5. AAH08036 90% 100% 184399 3481061 HKAAH36 838068 752 HMMER PFAM: Trypsin PF00089 270.2 452 1108 2.1.1 WUblastx.64 (AAH08036) Kallikrein 5. AAH08036 92% 254 1132 HKAAH36 815661 753 HMMER PFAM: Trypsin PF00089 270.2 327 983 2.1.1 WUblastx.64 (AAH08036) Kallikrein 5. AAH08036 100% 129 1007 HKAAH36 590734 754 WUblastx.64 (AAH08036) Kallikrein 5. AAH08036 100% 86% 189301 3531065 HKAAK02 589945 271 HMMER PFAM: Galactosyltransferase PF01762 56.1 457 660 2.1.1 WUblastx.64 (Q8WWR6) Beta 1,6-GlcNAc- Q8WWR6 92% 97 681 transferase. HKABZ65 862030 273 WUblastx.64 (Q96LB9) Peptidoglycan recognition Q96LB9 99% 45% 77137 802541 protein-I-alpha precursor. HKABZ65 665424 755 WUblastx.64 (Q96LB9) Peptidoglycan recognition Q96LB9 99% 45% 69129 794533 protein-I-alpha precursor. HKACB56 554616 274 HMMER PFAM: Kazal-type serine protease PF00050 76.3 114 266 2.1.1 inhibitor domain WUblastx.64 (P01001) ACROSIN INHIBITORS IAC2_BOVIN 82% 96 266 IIA AND IIB (BUSI-II). HKACD58 1352202 275 WUblastx.64 (Q96BH2) Hypothetical 34.4 kDa Q96BH2 86% 28% 100% 78646125 1199186715 protein. HKACD58 552465 756 WUblastx.64 (Q96BH2) Hypothetical 34.4 kDa Q96BH2 86% 28% 88% 79543122 1208183724 protein. HKACM93 1352383 277 blastx.14 aqualysin (EC 3.4.21.—) I precursor - pir|A35742|A35742 40% 41% 30% 884109712 103912761 Thermus aquaticus 50% 34% 747465484 468823670 53% 58% 252201 4692236 HKACM93 907085 758 WUblastx.64 aqualysin (EC 3.4.21.—) I precursor - pir|A35742|A35742 42% 35% 937521 1071919 Thermus aquaticus HKACM93 906150 760 WUblastx.64 (P80146) EXTRACELLULAR SEPR_THESR 39% 40 603 SERINE PROTEINASE PRECURSOR (EC 3.4. HKAEL80 570865 278 WUblastx.64 (O60448) NEURONAL THREAD O60448 63% 68% 65% 789934798 9359991052 PROTEIN AD7C-NTP. HKAEV06 1352263 279 WUblastx.64 (Q9NVA4) CDNA FLJ10846 FIS, Q9NVA4 99% 501 1814 CLONE NT2RP4001373. HKAEV06 638238 761 WUblastx.64 (Q9NVA4) CDNA FLJ10846 FIS, Q9NVA4 96% 100% 367197480 4593671541 CLONE NT2RP4001373. HKAFK41 545018 280 WUblastx.64 (BAB55101) CDNA FLJ14515 fis, BAB55101 91% 60% 18130 371537 clone NT2RM1000800, w HKAFT66 946512 281 WUblastx.64 (Q9CPS2) 4933428I03RIK Q9CPS2 72% 64% 84% 2961274 61231828 PROTEIN. HKAFT66 889258 762 WUblastx.64 (Q9CPS2) 4933428I03RIK Q9CPS2 72% 64% 83% 2961274 61231828 PROTEIN. HKAFT66 904790 763 WUblastx.64 (Q9CPS2) 4933428I03RIK Q9CPS2 80% 84% 29812 555314 PROTEIN. HKDBF34 833065 282 WUblastx.64 (Q9HBJ8) KIDNEY-SPECIFIC Q9HBJ8 88% 69 734 MEMBRANE PROTEIN NX-17. HKDBF34 587268 764 WUblastx.64 (Q9HBJ8) KIDNEY-SPECIFIC Q9HBJ8 100% 80% 18239 257682 MEMBRANE PROTEIN NX-17. HKGAT94 762811 283 WUblastx.64 (Q9H919) CDNA FLJ13078 FIS, Q9H919 73% 80% 63% 307128228 23984121 CLONE NT2RP3002002. HKGAT94 460631 765 WUblastx.64 (Q9H919) CDNA FLJ13078 FIS, Q9H919 73% 54% 80% 314105613 246907911 CLONE NT2RP3002002. 63% 5235 28 HKISB57 625956 285 WUblastx.64 (Q8WWW1) Smoothelin-B3. Q8WWW1 28% 100% 262201110 582101312 98% 27% 26% 7271532954 564809661 44% 052 HKMLM11 514788 287 WUblastx.64 (Q9P059) HSPC323 (FRAGMENT). Q9P059 71% 85% 332148 562462 HKMLP68 1037919 288 WUblastx.64 (Q8VD01) Hypothetical 61.8 kDa Q8VD01 49% 8 586 protein. HKMLP68 880047 767 WUblastx.64 (Q8VD01) Hypothetical 61.8 kDa Q8VD01 49% 31 609 protein. HKMND01 527402 290 WUblastx.64 (Q9H3C0) PRO0898. Q9H3C0 83% 867 757 HL2AC08 610018 291 HMMER PFAM: Thioredoxin PF00085 82.8 145 444 2.1.1 WUblastx.64 hypothetical protein pir|T12471|T12471 100% 46 903 DKFZp564E1962.1 - human (fragment) HLCND09 1172046 293 HMMER PFAM: PAP2 superfamily PF01569 20.3 170 352 2.1.1 WUblastx.64 (Q9H929) CDNA FLJ13055 FIS, Q9H929 88% 107 421 CLONE NT2RP3001538, WEAKLY SIMILAR TO HYP HLCND09 1035153 769 HMMER PFAM: PAP2 superfamily PF01569 20.4 62 244 2.1.1 WUblastx.64 (Q9H929) CDNA FLJ13055 FIS, Q9H929 97% 2 274 CLONE NT2RP3001538, WEAKLY SIMILAR TO HYP HLDBE54 836041 294 WUblastx.64 (Q9NR71) MITOCHONDRIAL Q9NR71 98% 212 1051 CERAMIDASE. HLDBE54 600362 770 WUblastx.64 (Q9JHE3) NERUTAL Q9JHE3 45% 72% 78% 332130375 3973061028 CERAMIDASE (NEUTRAL CERAMIDASE). HLDBE54 800678 771 HMMER PFAM: Renal dipeptidase PF01244 466.8 352 1410 2.1.1 WUblastx.64 (Q9H4A9) PUTATIVE Q9H4A9 100% 133 1590 DIPEPTIDASE. HLDBX13 815665 295 WUblastx.64 (Q9H387) PRO2550. Q9H387 76% 60% 17641815 16811756 HLDNA86 1352197 296 WUblastx.64 (Q9BQB6) UNKNOWN (PROTEIN Q9BQB6 100% 238 726 FOR MGC: 11276) (PROTEIN FOR IMAGE: 3455200). HLDNA86 535730 772 WUblastx.64 (Q9BQB6) UNKNOWN (PROTEIN Q9BQB6 72% 83% 100% 32621745 424339218 FOR MGC: 11276) (PROTEIN FOR IMAGE: 3455200). HLDOW79 847396 298 WUblastx.64 (AAH24441) Hypothetical 37.8 kDa AAH24441 83% 10 699 protein. HLDQC46 847397 299 WUblastx.64 (Q9BXJ8) TRANSMEMBRANE Q9BXJ8 100% 28 423 PROTEIN INDUCED BY TUMOR NECROSIS FACTOR ALPHA HLDQR62 753742 300 WUblastx.64 (Q9NQW2) PROGRESSIVE Q9NQW2 100% 99% 41376 3821002 ANKYLOSIS-LIKE PROTEIN. HLDQU79 740755 301 WUblastx.64 (O75477) KE04P. O75477 100% 105 1142 HLDRM43 846330 302 WUblastx.64 (Q96NZ9) Proline-rich acidic Q96NZ9 100% 24 476 protein. HLDRM43 638939 773 WUblastx.64 (Q96NZ9) Proline-rich acidic Q96NZ9 100% 164 616 protein. HLDRP33 647430 303 WUblastx.64 (Q9H743) CDNA: FLJ21394 FIS, Q9H743 38% 64% 340599 278489 CLONE COL03536. HLHFP03 460467 304 WUblastx.64 (Q9WVC2) LY-6/NEUROTOXIN Q9WVC2 81% 224 571 HOMOLOG (ADULT MALE HIPPOCAMPUS CDNA, RIKEN HLHFR58 894001 776 WUblastx.64 macrophage inflammatory protein 1- pir|JH0319|A31767 100% 610 335 beta precursor [validated] - human HLICQ90 791828 307 WUblastx.64 (Q96N65) CDNA FLJ31349 fis, Q96N65 95% 93% 57159 636616 clone MESAN2000092, moderately similar to HLQBE09 520375 309 WUblastx.64 second peroxisomal thioesterase - pir|JC7367|JC7367 56% 8 559 human HLQDR48 1307726 310 WUblastx.64 (Q9NQZ1) HEPATOCELLULAR Q9NQZ1 86% 296 406 CARCINOMA ASSOCIATED PROTEIN TD26. HLQDR48 619979 777 WUblastx.64 (AAH24408) Hypothetical 20.3 kDa AAH24408 65% 100% 54675 572701 protein (Fragment) HLTAU74 853614 311 WUblastx.64 (Q8WU84) Hypothetical 113.9 kDa Q8WU84 77% 100% 6657 704803 protein (Fragment). HLTEJ06 543017 314 WUblastx.64 (AAL78047) Envelope protein. AAL78047 32% 173 490 HLTHG37 787530 316 WUblastx.64 (AAH01258) N-acetylglucosamine- AAH01258 100% 93% 9602 1070955 phosphate mutase. HLTHG37 743169 778 WUblastx.64 (Q9NTT5) DJ202D23.2 (NOVEL Q9NTT5 100% 640 335 PROTEIN) (FRAGMENT). HLWAA17 629552 317 WUblastx.64 (Q9NY26) IRT1 PROTEIN Q9NY26 94% 100% 22685 960123 (SIMILAR TO ZINC/IRON REGULATED TRANSPORTER- LIK HLWAA88 588485 318 WUblastx.64 (Q9H8L6) CDNA FLJ13465 FIS, Q9H8L6 99% 99% 40% 683295781 176869685 CLONE PLACE1003493, 42% 92% 44035 5517322 WEAKLY SIMILAR TO END HLWAA88 769166 779 WUblastx.64 (Q9H8L6) CDNA FLJ13465 FIS, Q9H8L6 95% 93% 98% 1567148751 162915731 CLONE PLACE1003493, 493 WEAKLY SIMILAR TO END HLWAD77 653513 319 WUblastx.64 (Q9GZP9) F-LAN-1 Q9GZP9 99% 29 745 (HYPOTHETICAL TRANSMEMBRANE PROTEIN SBBI53). HLWAE11 783071 320 HMMER PFAM: C1q domain PF00386 44.4 403 789 2.1.1 WUblastx.64 (Q9BXI9) COMPLEMENT-C1Q Q9BXI9 99% 28 861 TUMOR NECROSIS FACTOR- RELATED PROTEIN. HLWAO22 587270 321 WUblastx.64 (Q9NRG9) GL003 (ADRACALIN) Q9NRG9 78% 28% 97% 449139100 114742012 (AAAS PROTEIN) (UNKNOWN) 100% 83% 314193965 634049559 (PROTEIN FOR MGC: 30% 41% 031004703 666440885 28% 26% 33 9503 58% HLWAY54 658702 322 WUblastx.64 (Q9BY87) PROACROSIN Q9BY87 99% 79% 100% 389971448 100613261 BINDING PROTEIN SP32 42% 23% 563144512 663643159 PRECURSOR. 37% 90% 601251 413311475 HLWBH18 1045194 323 WUblastx.64 (Q96MM0) CDNA FLJ32172 fis, Q96MM0 69% 594 722 clone PLACE6000555. HLWBK05 765310 325 WUblastx.64 (Q9CUS9) 4833416I09RIK Q9CUS9 84% 10 1173 PROTEIN (FRAGMENT). HLWBY76 797609 326 WUblastx.64 (AAH06651) Similar to hypothetical AAH06651 76% 6 1127 protein FLJ23153 HLYAN59 553507 781 WUblastx.64 (AAL79706) Hypothetical 9.4 kDa AAL79706 85% 93% 82% 624639617 719728721 protein. HLYAZ61 1352163 332 WUblastx.64 (O14626) PROBABLE G H963_HUMAN 100% 1 855 PROTEIN-COUPLED RECEPTOR H963. HLYAZ61 423998 782 HMMER PFAM: 7 transmembrane receptor PF00001 71.8 280 −283 2.1.1 (rhodopsin family) WUblastx.64 (O14626) PROBABLE G H963_HUMAN 98% 1 846 PROTEIN-COUPLED RECEPTOR H963. HLYES38 638042 334 WUblastx.64 (O95662) POT. ORF VI O95662 81% 72% 72% 743281306 856313524 (FRAGMENT). 75% 33% 466145 735243 HMADS41 596831 335 WUblastx.64 (AAH07725) Ceroid-lipofuscinosis, AAH07725 92% 100% 186427 4491041 neuronal 8 (epile HMADU73 1352177 336 WUblastx.64 (Q9EPE8) LOW-DENSITY Q9EPE8 87% 491 2626 LIPOPROTEIN RECEPTOR- RELATED PROTEIN 9. HMADU73 467053 783 WUblastx.64 (Q9EPE8) LOW-DENSITY Q9EPE8 78% 115 294 LIPOPROTEIN RECEPTOR- RELATED PROTEIN 9. HMAMI15 1352406 337 WUblastx.64 (AAL84703) Citrate lyase beta AAL84703 99% 4 1023 subunit. HMAMI15 1049263 784 WUblastx.64 (AAL84703) Citrate lyase beta AAL84703 100% 79% 3372 440920 subunit. HMDAE65 520338 338 WUblastx.64 (Q9NLE3) PROBABLE (HHV-6) Q9NLE3 79% 70% 63% 335342333 249250235 U1102, VARIANT A DNA, 64% 67% 330333 235250 COMPLETE VIRION GENOM HMDAM24 514394 339 WUblastx.64 hypothetical protein pir|T42663|T42663 92% 45% 33% 155298248 325363316 DKFZp434N0615.1 - human 31% 52% 345877369 962984764 (fragment) 26% 25% 158318306 298818926 31% 67% HMEAI48 1352290 341 WUblastx.64 (Q9Y639) STROMAL CELL- Q9Y639 80% 36 158 DERIVED RECEPTOR-1 ALPHA. HMECK83 636035 342 WUblastx.64 (O62658) LINE-1 ELEMENT O62658 32% 50% 49% 66865483 4836100 ORF2. HMEET96 566720 343 WUblastx.64 (Q9CR48) 2610318G18RIK Q9CR48 86% 121 915 PROTEIN. HMIAL37 603201 344 HMMER PFAM: PDZ domain (Also known as PF00595 57.7 127 327 2.1.1 DHR or GLGF). WUblastx.64 (Q9Y6N9) ANTIGEN NY-CO-38. Q9Y6N9 100% 100% 315761098 110031531 38% 27% 707651111 810619981 35% 62% 1067 2421132 63% HMIAP86 726831 345 HMMER PFAM: Mitochondrial carrier PF00153 262 329 1180 2.1.1 proteins WUblastx.64 (AAG29582) Mitochondrial AAG29582 97% 182 1183 uncoupling protein 5 long HMMAH60 562776 347 WUblastx.64 (Q9H728) CDNA: FLJ21463 FIS, Q9H728 52% 53% 675820 538665 CLONE COL04765. HMSBX80 597448 349 WUblastx.64 (Q9H728) CDNA: FLJ21463 FIS, Q9H728 55% 1721 1413 CLONE COL04765. HMSGB14 570833 351 WUblastx.64 (Q9BGV8) HYPOTHETICAL 10.0 KDA Q9BGV8 73% 403 615 PROTEIN. HMSGT42 383470 352 WUblastx.64 (Q9GZW0) DJ604K5.1 (15 KDA Q9GZW0 99% 40 525 SELENOPROTEIN). HMSHS36 1127691 354 WUblastx.64 (O95662) POT. ORF VI O95662 83% 781 350 (FRAGMENT). HMSHS36 1028961 786 WUblastx.64 (Q9H8K5) CDNA FLJ13501 FIS, Q9H8K5 64% 78% 79% 94340367 544381489 CLONE PLACE1004815. HMSKC04 799540 357 WUblastx.64 (Q9H743) CDNA: FLJ21394 FIS, Q9H743 66% 60% 56% 134114141 122513461 CLONE COL03536. 244 053 HMTBI36 1301451 358 WUblastx.64 (Q9VZF8) CG1332 PROTEIN. Q9VZF8 56% 36% 40% 958248837 255630248 35% 27% 623412494 792550262 40% 712 2834 HMTBI36 866466 787 HMMER PFAM: WD domain, G-beta repeat PF00400 45.8 2490 2600 2.1.1 WUblastx.64 (Q9VZF8) CG1332 PROTEIN. Q9VZF8 56% 36% 40% 957248737 255530238 35% 27% 523402493 782549262 40% 711 1833 HMUAP70 872208 359 WUblastx.64 (Q9EQH8) NEDD4 WW DOMAIN- Q9EQH8 89% 69 845 BINDING PROTEIN 5 (FRAGMENT). HMUAP70 723302 788 WUblastx.64 (Q9BT67) UNKNOWN (PROTEIN Q9BT67 73% 99% 60107 104721 FOR MGC: 10924). HMUAP70 778820 789 WUblastx.64 (Q9BT67) UNKNOWN (PROTEIN Q9BT67 100% 72% 183229338 221402844 FOR MGC: 10924). 100% HMUAP70 674913 790 WUblastx.64 (Q9BT67) UNKNOWN (PROTEIN Q9BT67 98% 94% 82% 20910962 379216112 FOR MGC: 10924). HMUAP70 646810 791 WUblastx.64 (Q9BT67) UNKNOWN (PROTEIN Q9BT67 73% 96% 60107 104583 FOR MGC: 10924). HMUAP70 381964 792 WUblastx.64 (Q9BT67) UNKNOWN (PROTEIN Q9BT67 86% 99% 60106 104720 FOR MGC: 10924). HMWEB02 638159 361 WUblastx.64 (Q96MX0) CDNA FLJ31762 fis, Q96MX0 100% 34% 61187333 207300449 clone NT2RI2007754, weakly 97% similar to INT HMWFO02 542061 793 WUblastx.64 (Q9P1C6) PRO2738. Q9P1C6 61% 44% 647473 549345 HMWGY65 1308287 363 WUblastx.64 (Q8VCP9) RIKEN cDNA Q8VCP9 66% 42 1442 1200003C23 gene. HMWGY65 794987 794 WUblastx.64 (Q8VCP9) RIKEN cDNA Q8VCP9 58% 65% 54242 1438596 1200003C23 gene. HNEEB45 1036397 365 WUblastx.64 hypothetical protein 3 - human pir|E41925|E41925 78% 39% 44% 861523548 929717862 HNFFC43 753337 366 WUblastx.64 (Q969J4) Lipocalin-1 interacting Q969J4 97% 66% 87% 319428651 453769839 membrane receptor (Lipocalin- 99% 903 1517 interac HNFIU96 460611 367 WUblastx.64 (Q26195) PVA1 GENE. Q26195 66% 54% 61% 331177318 366323371 HNFJF07 577013 368 WUblastx.64 (Q8WYX2) Hypothetical 14.1 kDa Q8WYX2 65% 585 457 protein. HNFJH45 410107 369 WUblastx.64 (Q9H7Z0) CDNA FLJ14058 FIS, Q9H7Z0 48% 277 11 CLONE HEMBB1000554. HNGAK47 561488 370 WUblastx.64 (Q96EF8) Unknown (protein for Q96EF8 33% 31% 20% 121249249 206206617 MGC: 21495). 34% 25% 2486190537 5575692487 39% 29% HNGEP09 499076 378 WUblastx.64 (AAK55521) PRO0764. AAK55521 57% 53% 50% 9651021867 861977715 HNGIJ31 519120 381 WUblastx.64 (Q9N083) UNNAMED PORTEIN Q9N083 73% 54% 66% 566615454 610725561 PRODUCT. HNGJE50 561568 383 WUblastx.64 (Q9HBS7) HYPOTHETICAL 14.2 KDA Q9HBS7 64% 62% 1028919 945734 PROTEIN. HNGJP69 604891 385 WUblastx.64 (Q9H743) CDNA: FLJ21394 FIS, Q9H743 53% 71% 973860 857693 CLONE COL03536. HNGKN89 834857 387 WUblastx.64 (Q9BGZ4) HYPOTHETICAL 11.6 KDA Q9BGZ4 67% 891 781 PROTEIN. HNGOM56 836064 388 WUblastx.64 (Q96MM0) CDNA FLJ32172 fis, Q96MM0 38% 58% 577714 744953 clone PLACE6000555. HNHFO29 463568 399 WUblastx.64 (Q9NX85) CDNA FLJ20378 FIS, Q9NX85 69% 522 695 CLONE KAIA0536. HNHOD46 843488 402 WUblastx.64 (O60448) NEURONAL THREAD O60448 76% 56% 56% 334646645 552921713 PROTEIN AD7C-NTP. 52% 73% 844331353 894498625 59% 50% 828721781 917792915 70% 48% 558401283 791595552 50% 35% 379486 462839 31% 50% 61% HNTBI57 570877 405 WUblastx.64 (O95400) CD2 CYTOPLASMIC O95400 100% 173 1195 DOMAIN BINDING PROTEIN (CD2 ANTIGEN (CYTOPLA HNTCE26 1160395 406 HMMER PFAM: 7 transmembrane receptor PF00001 137.5 282 1037 2.1.1 (rhodopsin family) WUblastx.64 (Q9H1Y3) DJ317G22.2 Q9H1Y3 100% 111 1316 (ENCEPHALOPSIN) (PANOPSIN). HNTCE26 853373 802 HMMER PFAM: 7 transmembrane receptor PF00001 23.2 63 218 2.1.1 (rhodopsin family) WUblastx.64 (Q9H1Y3) DJ317G22.2 Q9H1Y3 95% 100% 37012 495377 (ENCEPHALOPSIN) (PANOPSIN). HNTNC20 700627 407 WUblastx.64 (AAH24118) Similar to Unknown AAH24118 57% 252 776 (protein for IMAGE: 44 HNTSY18 1041383 409 WUblastx.64 (Q9XSV8) SCO-SPONDIN Q9XSV8 70% 63% 37% 511204546 644123659 (FRAGMENT). 31% 29% 682442664 680393159 28% 30% 841663510 686366292 36% 30% 781482110 212761356 29% 29% 153953022 151711571 41% 50% 875584379 201892584 78% 26% 159954661 119855153 36% 26% 4851017 732938932 29% 33% 958115231 32% 34% 076 30% 25% 42% 40% HNTSY18 897950 804 WUblastx.64 (Q9GMX5) HYPOTHETICAL 12.9 KDA Q9GMX5 61% 356 201 PROTEIN. HOACB38 520201 411 WUblastx.64 (Q9H387) PRO2550. Q9H387 71% 77% 420589 295419 HODDN65 520348 414 WUblastx.64 (Q9N083) UNNAMED PORTEIN Q9N083 74% 67% 743660 663493 PRODUCT. HODDN92 422913 415 WUblastx.64 (Q9H1S5) BA110H4.2 (SIMILAR Q9H1S5 100% 1119 1021 TO MEMBRANE PROTEIN). HODDO08 790333 416 WUblastx.64 (Q8WZ36) Hypothetical 11.9 kDa Q8WZ36 83% 725 1042 protein. HODDW40 579256 417 WUblastx.64 (Q9GMP5) HYPOTHETICAL 6.6 KDA Q9GMP5 60% 657 520 PROTEIN. HODGE68 834907 420 WUblastx.64 retrovirus-related hypothetical pir|S23650|S23650 36% 54% 370276 2781 protein II - human 1 HOEBK34 768325 421 HMMER PFAM: von Willebrand factor type PF00093 54.1 455 619 2.1.1 C domain WUblastx.64 (O94769) EXTRACELLULAR O94769 90% 149 643 MATRIX PROTEIN. HOEBK34 509951 807 WUblastx.64 (O94769) EXTRACELLULAR O94769 96% 93% 68316 325561 MATRIX PROTEIN. HOEBZ89 828177 422 WUblastx.64 hypothetical protein C05G5.5 - pir|T18967|T18967 31% 133 969 Caenorhabditis elegans HOEDB32 634994 423 WUblastx.64 (Q9Y2Y6) TADA1 PROTEIN Q9Y2Y6 100% 104 781 (DKFZP564K1964 PROTEIN). HOEDE28 1036480 424 WUblastx.64 (Q8WY86) PP3686. Q8WY86 99% 933 1535 HOEDH84 748236 425 WUblastx.64 (Q960D8) SD05564p. Q960D8 39% 7 1449 HOEFV61 833079 426 HMMER PFAM: Leucine Rich Repeat PF00560 22 142 216 2.1.1 WUblastx.64 (Q9C000) NAC-BETA SPLICE Q9C000 97% 94% 36% 695149611 150719691 VARIANT. 100% 57% 631014193 300555146 29% 100% 031945127 043420014 44% 34% 555206541 896595053 30% 29% 09549 83546704 30% 96% HOFMQ33 1184465 427 WUblastx.64 (O15232) MATRILIN-3 MTN3_HUMAN 85% 43 1500 PRECURSOR. HOFMQ33 919896 809 HMMER PFAM: von Willebrand factor type PF00092 189.8 288 815 2.1.1 A domain WUblastx.64 (O15232) MATRILIN-3 MTN3_HUMAN 85% 42 1499 PRECURSOR. HOFMQ33 906694 810 HMMER PFAM: von Willebrand factor type PF00092 162.2 318 737 2.1.1 A domain WUblastx.64 (O15232) MATRILIN-3 MTN3_HUMAN 81% 72 857 PRECURSOR. HOFMQ33 902639 811 WUblastx.64 (O15232) MATRILIN-3 MTN3_HUMAN 81% 1584 877 PRECURSOR. HOFMQ33 702186 812 WUblastx.64 (Q8WUF2) Hypothetical 23.7 kDa Q8WUF2 88% 99% 937914 911327 protein. HOFMT75 911180 428 HMMER PFAM: Eukaryotic aspartyl protease PF00026 619 290 1303 2.1.1 WUblastx.64 cathepsin D (EC 3.4.23.5) precursor pir|A25771|KHHUD 87% 83 1312 [validated]- human HOFMT75 905365 813 WUblastx.64 cathepsin D (EC 3.4.23.5) precursor pir|A25771|KHHUD 65% 83 361 [validated]- human HOFMT75 892308 814 WUblastx.64 cathepsin D (EC 3.4.23.5) precursor pir|A25771|KHHUD 88% 1494 757 [validated]- human HOFMT75 892291 815 HMMER PFAM: Eukaryotic aspartyl protease PF00026 496.2 336 1232 2.1.1 WUblastx.64 cathepsin D (EC 3.4.23.5) precursor pir|A25771|KHHUD 99% 129 1232 [validated] - human HOFND85 847424 430 HMMER PFAM: Cadherin domain PF00028 256 905 1180 2.1.1 WUblastx.64 (AAK51617) Protocadherin-beta7. AAK51617 83% 30% 167425 20471858 HOFOC33 1186156 432 WUblastx.64 clusterin precursor - dog pir|A40018|A40018 69% 81% 1022115 14141086 HOFOC33 967554 817 HMMER PFAM: Clusterin PF01093 236.4 81 395 2.1.1 WUblastx.64 clusterin precursor - dog pir|A40018|A40018 44% 91% 37381 453395 HOFOC33 878690 818 HMMER PFAM: Clusterin PF01093 236.6 81 395 2.1.1 WUblastx.64 clusterin precursor - dog pir|A40018|A40018 44% 91% 37381 453395 HOFOC33 905734 819 HMMER PFAM: Clusterin PF01093 301.2 76 432 2.1.1 WUblastx.64 clusterin precursor - dog pir|A40018|A40018 77% 95% 86% 102376440 141543210 87 HOFOC33 902326 820 WUblastx.64 clusterin precursor - dog pir|A40018|A40018 84% 583 257 HOFOC33 885140 821 WUblastx.64 clusterin precursor - dog pir|A40018|A40018 77% 839 36 HOFOC33 806819 822 HMMER PFAM: 60s Acidic ribosomal protein PF00428 74.6 −422 −733 2.1.1 WUblastx.64 acidic ribosomal protein P0, pir|A27125|R5HUP0 52% 87% 542 55812 cytosolic [validated] - human HOFOC73 931871 433 HMMER PFAM: Papain family cysteine PF00112 22.3 192 311 2.1.1 protease WUblastx.64 (BAB22302) Adult male kidney BAB22302 87% 70% 31618 918341 cDNA, RIKEN full-lengt HOFOC73 907073 823 WUblastx.64 (CAC09370) DJ543J19.3 (cathepsin CAC09370 76% 84% 64411 414920 Z). HOFOC73 878863 825 WUblastx.64 (BAB55004) CDNA FLJ14357 fis, BAB55004 100% 2291 819 clone HEMBA1000005, h HOGAW62 579891 434 WUblastx.64 (Q8WUD4) Similar to RIKEN Q8WUD4 100% 35 130 cDNA 2700094L05 gene. HOGCK20 745445 435 WUblastx.64 (Q969N2) Phosphatidyl inositol Q969N2 99% 97% 37857 1622389 glycan class T precursor (Hypothetical HOGCK20 664499 826 WUblastx.64 (Q969N2) Phosphatidyl inositol Q969N2 92% 97% 44% 153368515 161638212 glycan class T precursor 50% 99% 2371 5811534 (Hypothetical HOGCK63 895880 436 WUblastx.64 (Q9Y386) CGI-78 PROTEIN. Q9Y386 76% 88% 100% 121411615 126412141 14 161 HOGCK63 902295 827 WUblastx.64 (Q96BI3) Hypothetical 29.0 kDa Q96BI3 100% 96% 81322 872477 protein (CGI-78 protein). HOGCS52 919898 437 WUblastx.64 (Q9NY68) CTL2 PROTEIN. Q9NY68 99% 31 1383 HOGCS52 907118 828 WUblastx.64 (Q9NY68) CTL2 PROTEIN. Q9NY68 99% 36 1388 HOGCS52 867965 829 WUblastx.64 (Q9H728) CDNA: FLJ21463 FIS, Q9H728 59% 74% 1017931 952719 CLONE COL04765. HOHBB49 833080 438 WUblastx.64 (Q9UI50) PRO0657 (FRAGMENT). Q9UI50 71% 60% 22942374 23562493 HOHBC68 603968 439 WUblastx.64 (Q8WUJ3) Hypothetical 110.4 kDa Q8WUJ3 94% 97% 348676 7071785 protein. HOHBY44 873264 441 WUblastx.64 (O60565) GREMLIN (DRM). O60565 100% 170 721 HOHCH55 827481 443 WUblastx.64 (O95965) TEN INTEGRIN EGF- O95965 100% 221 1702 LIKE REPEAT DOMAINS PROTEIN PRECURSOR. HOHCH55 815682 832 WUblastx.64 (O95965) TEN INTEGRIN EGF- O95965 100% 31% 162341623 171215761 LIKE REPEAT DOMAINS 99% 40% 0326 6211426 PROTEIN PRECURSOR. HONAH29 1299928 444 WUblastx.64 (Q9NWM8) CDNA FLJ20731 FIS, Q9NWM8 100% 136 768 CLONE HEP10272 (HYPOTHETICAL 24.2 KDA PRO HONAH29 457167 833 HMMER PFAM: FKBP-type peptidyl-prolyl PF00254 95.1 288 539 2.1.1 cis-trans isomerases WUblastx.64 (Q9NWM8) CDNA FLJ20731 FIS, Q9NWM8 98% 144 776 CLONE HEP10272 (HYPOTHETICAL 24.2 KDA PRO HOSDJ25 854234 445 WUblastx.64 (Q9D8Y9) 1810018L05RIK Q9D8Y9 85% 86% 468143 593544 PROTEIN. HOSEG51 545809 446 WUblastx.64 (Q9NUT5) CDNA FLJ11152 FIS, Q9NUT5 51% 100% 246 82537 CLONE PLACE1006901 (FRAGMENT). HOSFD58 614040 447 HMMER PFAM: ATP-sulfurylase PF01747 697.3 −647 −1633 2.1.1 WUblastx.64 3′-phosphoadenosine-5′- pir|JW0087|JW0087 100% 56 1927 phosphosulfate synthetase - human HOSFD58 383513 835 WUblastx.64 3′-phosphoadenosine-5′- pir|JW0087|JW0087 100% 56 1927 phosphosulfate synthetase - human HOUCQ17 429229 448 HMMER PFAM: Reprolysin family PF01562 76.2 216 −20 2.1.1 propeptide WUblastx.64 (P97857) ADAM-TS 1 ATS1_MOUSE 81% 508 3408 PRECURSOR (EC 3.4.24.—) (A DISINTEGRIN A HOUDK26 565393 449 WUblastx.64 (Q9NUX1) CDNA FLJ11082 FIS, Q9NUX1 87% 4 585 CLONE PLACE1005206. HPASA81 1352382 451 WUblastx.64 (O35360) UTERUS-OVARY O35360 73% 1 1818 SPECIFIC PUTATIVE TRANSMEMBRANE PROTEIN. HPASA81 900548 836 HMMER PFAM: CUB domain PF00431 146.9 452 778 2.1.1 WUblastx.64 (O35360) UTERUS-OVARY O35360 67% 75% 8918 9281814 SPECIFIC PUTATIVE TRANSMEMBRANE PROTEIN. HPBCU51 411080 452 WUblastx.64 (Q9BWJ9) SIMILAR TO Q9BWJ9 96% 56 154 NEUROBLASTOMA (NERVE TISSUE) PROTEIN. HPFCL43 535710 457 WUblastx.64 (AAH07349) Adrenal gland protein AAH07349 97% 57 257 AD-004. HPFDG48 542227 458 WUblastx.64 (Q9Y6E5) HSPC024-ISO. Q9Y6E5 90% 88% 564313 623387 HPIAQ68 833082 459 WUblastx.64 (Q95LL4) Hypothetical 13.9 kDa Q95LL4 46% 905 1174 protein. HPIBO15 1310868 460 WUblastx.64 (Q9CQS3) 1110018M03RIK Q9CQS3 93% 128 757 PROTEIN. HPIBO15 590741 840 WUblastx.64 (Q9CQS3) 1110018M03RIK Q9CQS3 88% 95% 97% 127507401 402722508 PROTEIN. HPICB53 1042309 461 WUblastx.64 (Q9NX17) CDNA FLJ20489 FIS, Q9NX17 74% 1138 848 CLONE KAT08285. HPJCL22 1146674 463 WUblastx.64 (Q9GKV3) HYPOTHETICAL 41.8 KDA Q9GKV3 97% 27% 75% 142021027 250833828 PROTEIN. 01 23 HPJCL22 1034817 845 WUblastx.64 (Q9VWN8) CG7307 PROTEIN. Q9VWN8 69% 61% 64468 348992 HPJCL22 1046434 846 WUblastx.64 (Q9H8F3) CDNA FLJ13680 FIS, Q9H8F3 94% 81% 34616 582162 CLONE PLACE2000007, HIGHLY SIMILAR TO HOM HPJCW04 589969 464 WUblastx.64 (Q9P195) PRO1722. Q9P195 39% 60% 12781412 10931263 HPMAI22 635491 466 WUblastx.64 (Q9CX19) 9430073N08RIK Q9CX19 54% 147 572 PROTEIN. HPQAC69 396804 469 WUblastx.64 (O75592) PROTEIN ASSOCIATED O75592 100% 28% 202763 297189200 WITH MYC. 100% HPRBC80 829136 470 HMMER PFAM: Protein phosphatase 2C PF00481 336.4 157 957 2.1.1 WUblastx.64 (Q9HAY8) SER/THR PROTEIN Q9HAY8 99% 94 1254 PHOSPHATASE TYPE 2C BETA 2 ISOFORM (PROTEIN HPRBC80 720095 851 WUblastx.64 (Q9HAY8) SER/THR PROTEIN Q9HAY8 98% 3 284 PHOSPHATASE TYPE 2C BETA 2 ISOFORM (PROTEIN HPRBF19 753282 471 WUblastx.64 (Q9H817) CDNA FLJ13593 FIS, Q9H8I7 99% 15 632 CLONE PLACE1009493. HPTVX32 634353 473 WUblastx.64 (BAB84985) FLJ00232 protein BAB84985 96% 103 543 (Fragment). HPWDJ42 722246 476 WUblastx.64 (Q9H728) CDNA: FLJ21463 FIS, Q9H728 64% 67% 11001332 10261102 CLONE COL04765. HPWDJ42 709662 854 WUblastx.64 (Q9H728) CDNA: FLJ21463 FIS, Q9H728 64% 67% 11001332 10261102 CLONE COL04765. HPZAB47 585702 477 WUblastx.64 hypothetical protein 3 - human pir|E41925|E41925 34% 55% 11321296 8841183 HRAAB15 658717 478 WUblastx.64 (AAH25678) Similar to putative. AAH25678 100% 11 511 HRABA80 882176 479 WUblastx.64 (Q9HA75) CDNA FLJ12122 FIS, Q9HA75 63% 48% 93% 647144247 679371507 CLONE MAMMA1000129. HRABA80 588460 856 WUblastx.64 (Q9HA75) CDNA FLJ12122 FIS, Q9HA75 63% 48% 92% 633130233 665357493 CLONE MAMMA1000129. HRACD15 871221 480 WUblastx.64 (AAH08084) Hypothetical 50.4 kDa AAH08084 98% 1452 253 protein. HRACD15 706332 857 WUblastx.64 (AAH08084) Hypothetical 50.4 kDa AAH08084 82% 98% 16491596 1581253 protein. HRACD80 1309774 481 WUblastx.64 (CAC37630) Fibulin-6 (Fragment). CAC37630 44% 36% 45% 700371282 186614461 42% 47% 12911291 920158415 30 HRACD80 882163 858 HMMER PFAM: EGF-like domain PF00008 64.3 1337 1441 2.1.1 WUblastx.64 (CAC37630) Fibulin-6 (Fragment). CAC37630 44% 37% 45% 695321277 186114411 42% 47% 12861286 915157915 25 HRDDV47 637650 482 WUblastx.64 (Q9VXD6) CG9723 PROTEIN. Q9VXD6 27% 224 964 HRDFD27 567004 483 WUblastx.64 (Q9N032) UNNAMED PROTEIN Q9N032 47% 679 476 PRODUCT. HROAJ03 567005 484 WUblastx.64 (Q96A82) CDNA FLJ30106 fis, Q96A82 88% 7 786 clone BNGH41000190, weakly similar to Rat HSATR82 531973 486 WUblastx.64 (Q9UI58) PRO0483 PROTEIN. Q9UI58 80% 76% 678605 707682 HSAUL82 490879 488 WUblastx.64 (Q9BE22) HYPOTHETICAL 13.4 KDA Q9BE22 63% 546 701 PROTEIN. HSAVH65 545459 489 WUblastx.64 (Q9CZR4) 2700018N07RIK Q9CZR4 92% 23 403 PROTEIN. HSAVK10 561435 490 WUblastx.64 (Q9H728) CDNA: FLJ21463 FIS, Q9H728 70% 63% 10551218 9331030 CLONE COL04765. HSAWD74 460527 491 WUblastx.64 (Q9NX85) CDNA FLJ20378 FIS, Q9NX85 67% 967 674 CLONE KAIA0536. HSAWZ41 580872 492 WUblastx.64 (Q9H387) PRO2550. Q9H387 81% 1386 1102 HSAXA83 545051 493 WUblastx.64 (Q9NRX6) PROTEIN X 013. Q9NRX6 100% 92 313 HSAYB43 604143 494 WUblastx.64 (Q9N083) UNNAMED PORTEIN Q9N083 60% 50% 16621580 15731338 PRODUCT. HSDAJ46 692358 496 HMMER PFAM: Eukaryotic-type carbonic PF00194 163.5 362 793 2.1.1 anhydrase WUblastx.64 (Q9ULX7) CARBONIC CAHE_HUMAN 99% 98% 299791 7961084 ANHYDRASE XIV PRECURSOR (EC 4.2.1.1) (CAR HSDEK49 1352253 497 WUblastx.64 (Q9Y279) Z39IG PROTEIN Q9Y279 100% 60 1256 PRECURSOR. HSDEK49 625998 862 HMMER PFAM: Immunoglobulin domain PF00047 18.7 225 470 2.1.1 WUblastx.64 (Q9Y279) Z39IG PROTEIN Q9Y279 88% 99% 444126 1040542 PRECURSOR. HSDEZ20 1352287 499 WUblastx.64 probable voltage-activated cation pir|T17101|T17101 98% 4 336 channel - rat HSDEZ20 704101 863 WUblastx.64 probable voltage-activated cation pir|T17101|T17101 89% 9 335 channel - rat HSDFW45 589974 500 WUblastx.64 (Q9NX85) CDNA FLJ20378 FIS, Q9NX85 77% 1645 1352 CLONE KAIA0536. HSDJA15 795252 501 WUblastx.64 (Q9BZW5) TRANSMEMBRANE 6 Q9BZW5 99% 4 702 SUPERFAMILY MEMBER 1. HSDJL42 1036471 503 WUblastx.64 (Q9BVS2) UNKNOWN (PROTEIN Q9BVS2 65% 57 590 FOR IMAGE: 3451448) (FRAGMENT). HSDJL42 904821 864 WUblastx.64 (Q9BVS2) UNKNOWN (PROTEIN Q9BVS2 65% 6 539 FOR IMAGE: 3451448) (FRAGMENT). HSDJL42 905623 865 WUblastx.64 (Q9BVS2) UNKNOWN (PROTEIN Q9BVS2 64% 57 590 FOR IMAGE: 3451448) (FRAGMENT). HSDSE75 545057 506 WUblastx.64 (O60245) PCDH7 (BH-PCDH)A. O60245 100% 10 702 HSDZR57 651375 507 WUblastx.64 (Q9NX00) CDNA FLJ20512 FIS, Q9NX00 100% 9 209 CLONE KAT09739. HSHAX21 612823 508 WUblastx.64 (Q9NV22) CDNA FLJ10983 FIS, Q9NV22 99% 5 598 CLONE PLACE1001781, WEAKLY SIMILAR TO PRO HSIAS17 1352191 509 WUblastx.64 (Q9H6H4) CDNA: FLJ22277 FIS, Q9H6H4 100% 431 1201 CLONE HRC03740. HSIAS17 514183 867 WUblastx.64 (Q9H6H4) CDNA: FLJ22277 FIS, Q9H6H4 100% 96% 108350 362877 CLONE HRC03740. HSICV24 1352248 510 WUblastx.64 (Q96J88) Putative breast epithelial Q96J88 100% 153 884 stromal interaction protein. HSICV24 612877 868 WUblastx.64 (Q96J88) Putative breast epithelial Q96J88 100% 251 916 stromal interaction protein. HSIDJ81 589447 511 WUblastx.64 (Q9H728) CDNA: FLJ21463 FIS, Q9H728 74% 1289 996 CLONE COL04765. HSIDX71 1033671 512 WUblastx.64 (AAK55521) PRO0764. AAK55521 59% 65% 18291786 17641526 HSIDX71 902162 869 WUblastx.64 (AAK55521) PRO0764. AAK55521 59% 65% 18251782 17601522 HSJBQ79 1304677 513 WUblastx.64 (Q96D15) Hypothetical 37.5 kDa Q96D15 96% 38 586 protein. HSJBQ79 661698 870 HMMER PFAM: EF hand PF00036 23.4 663 734 2.1.1 WUblastx.64 (Q96D15) Hypothetical 37.5 kDa Q96D15 99% 54 1037 protein. HSJBQ79 371784 871 WUblastx.64 (Q96D15) Hypothetical 37.5 kDa Q96D15 97% 32 586 protein. HSKCP69 702021 514 WUblastx.64 (Q9H5G5) CDNA: FLJ23462 FIS, Q9H5G5 99% 49 906 CLONE HSI08475. HSKCP69 413210 872 WUblastx.64 (Q9H5G5) CDNA: FLJ23462 FIS, Q9H5G5 96% 98% 49234 243905 CLONE HSI08475. HSKDA27 1352409 515 WUblastx.64 (BAB85613) URB. BAB85613 83% 786 3635 HSKDA27 1074734 873 WUblastx.64 (BAB85613) URB. BAB85613 60% 60% 52% 160117151 178917891 73% 32% 7181271716 792179117 90 HSKDA27 872570 874 WUblastx.64 (BAB85613) URB. BAB85613 69% 32% 91597 16701671 HSODE04 906498 879 WUblastx.64 protein BYJ15 - common tobacco pir|T02229|T02229 36% 96% 107128 1136102 (fragment) HSQEO84 1306702 522 WUblastx.64 (Q96DA4) FK506-binding protein. Q96DA4 100% 75 740 HSQEO84 602258 880 HMMER PFAM: FKBP-type peptidyl-prolyl PF00254 92 −30 −326 2.1.1 cis-trans isomerases WUblastx.64 (Q96DA4) FK506-binding protein. Q96DA4 100% 79 744 HSQEO84 401251 881 WUblastx.64 (O54998) FK506-BINDING O54998 75% 86% 86216 241740 PROTEIN 7 PRECURSOR (EC 5.2.1.8) (FKBP-23) (PE HSSDX51 566879 524 WUblastx.64 (Q9NQ80) ASPIC PRECURSOR. Q9NQ80 83% 40% 72% 153011017 368399692 41% 32% 47899323 662512571 26% 87% 105 HSSGD52 1352343 526 WUblastx.64 (Q96FI8) Unknown (protein for Q96FI8 100% 344 2161 MGC: 9160). HSSGD52 845666 882 WUblastx.64 (Q96FI8) Unknown (protein for Q96FI8 100% 338 2155 MGC: 9160). HSSJC35 1306937 528 WUblastx.64 (Q9H400) DJ583P15.4.1 (NOVEL Q9H400 81% 62 946 PROTEIN (TRANSLATION OF CDNA FLJ20406 (E HSSJC35 745409 883 WUblastx.64 (Q9H400) DJ583P15.4.1 (NOVEL Q9H400 100% 55 939 PROTEIN (TRANSLATION OF CDNA FLJ20406 (E HSSJC35 716424 884 WUblastx.64 (Q9H400) DJ583P15.4.1 (NOVEL Q9H400 76% 69% 16166 949530 PROTEIN (TRANSLATION OF CDNA FLJ20406 (E HSUBW09 413246 530 WUblastx.64 (Q95LL0) Hypothetical 11.3 kDa Q95LL0 73% 77% 589327 633611 protein. HSVBU91 596868 533 WUblastx.64 cytoplasmic linker protein CLIP-115 - pir|T42734|T42734 85% 356 171 rat HSXCG83 944388 534 WUblastx.64 (Q9H7F4) CDNA: FLJ20979 FIS, Q9H7F4 93% 101 901 CLONE ADSU01938. HSXCG83 830673 885 WUblastx.64 (Q9H7F4) CDNA: FLJ20979 FIS, Q9H7F4 98% 4 726 CLONE ADSU01938. HSXGI47 886200 536 WUblastx.64 (Q9H728) CDNA: FLJ21463 FIS, Q9H728 56% 55% 585762 860965 CLONE COL04765. HSYAV50 847358 537 HMMER PFAM: Leucine Rich Repeat PF00560 97.9 383 454 2.1.1 WUblastx.64 (Q96CX1) Similar to RIKEN cDNA Q96CX1 96% 371 2170 2610528G05 gene (Fragment). HSYAZ50 902235 889 WUblastx.64 (Q96NR6) CDNA FLJ30278 fis, Q96NR6 70% 1945 2064 clone BRACE2002755. HSYAZ50 882732 890 WUblastx.64 (Q9NVZ3) CDNA FLJ10420 FIS, Q9NVZ3 100% 50 838 CLONE NT2RP1000170. HSYAZ63 1177537 540 WUblastx.64 (Q9Y613) FH1/FH2 DOMAINS- FHOS_HUMAN 98% 55% 81% 889272210 171354425 CONTAINING PROTEIN 100% 92% 147830072 147503090 (FORMIN HOMOLOG 28% 42% 896081015 654670145 28% 33% 203020052 821192052 56% 73% 573 2941 HSYAZ63 862063 891 WUblastx.64 (Q9Y613) FH1/FH2 DOMAINS- FHOS_HUMAN 69% 92% 73% 458136493 871144712 CONTAINING PROTEIN 52% 33% 036238714 9841847670 (FORMIN HOMOLOG 100% HSYBG37 1056317 541 WUblastx.64 hypothetical protein c316G12.3 pir|45062|T45062 100% 47 961 [imported] - human HSYBG37 581098 892 WUblastx.64 hypothetical protein c316G12.3 pir|T45062|T45062 100% 48 962 [imported] - human HSZAF47 1352172 542 WUblastx.64 (Q9BXJ2) COMPLEMENT-C1Q Q9BXJ2 100% 106 972 TUMOR NECROSIS FACTOR- RELATED PROTEIN. HSZAF47 456551 893 HMMER PFAM: Collagen triple helix repeat PF01391 54.4 299 478 2.1.1 (20 copies) WUblastx.64 (Q9BXJ2) COMPLEMENT-C1Q Q9BXJ2 92% 107 976 TUMOR NECROSIS FACTOR- RELATED PROTEIN. HT3SF53 884170 543 WUblastx.64 (Q9H5B4) DJ470L14.2.1 Q9H5B4 100% 312 533 (STAUFEN (RNA BINDING PROTEIN) ISOFORM 1). HT5GJ57 1299921 544 WUblastx.64 (Q9GZY6) CDNA FLJ11237 FIS, Q9GZY6 89% 105 833 CLONE PLACE1008531 (WBSCR5) (WBSCR15 PROT HT5GJ57 740767 894 WUblastx.64 (Q9GZY6) CDNA FLJ11237 FIS, Q9GZY6 84% 122 856 CLONE PLACE1008531 (WBSCR5) (WBSCR15 PROT HTADW91 844835 545 WUblastx.64 (Q8WV10) Hypothetical 38.4 kDa Q8WV10 86% 155 1117 protein. HTADX17 753289 546 WUblastx.64 (Q96A28) CD84-H1 (CD2 FAMILY Q96A28 100% 99% 92408 412959 10). HTADX17 457172 895 WUblastx.64 (Q96A28) CD84-H1 (CD2 FAMILY Q96A28 78% 97% 9% 49054884 585952488 10). HTAEE28 1018291 547 WUblastx.64 (Q9D4I2) 4932408F18RIK Q9D4I2 78% 319 1161 PROTEIN. HTAEE28 882919 896 WUblastx.64 (Q9D4I2) 4932408F18RIK Q9D4I2 78% 372 617 PROTEIN. HTAEE28 864120 897 WUblastx.64 (Q9D4I2) 4932408F18RIK Q9D4I2 76% 142 768 PROTEIN. HTDAF28 396835 548 WUblastx.64 (Q9BX79) STRA6 ISOFORM 1. Q9BX79 98% 17 298 HTEAF65 866485 549 WUblastx.64 (AAH25354) Similar to putative. AAH25354 100% 9 257 HTEBI28 462221 550 WUblastx.64 (Q95LI0) Epididymis-specific Q95LI0 46% 43 231 protein ESP13.6. HTEDF80 587326 551 WUblastx.64 (Q9NP89) HYPOTHETICAL 42.7 KDA Q9NP89 100% 91% 253353852 327451107 PROTEIN (FRAGMENT). 100% 75% 112698450 3210856863 98% 66% HTEDY42 1352193 552 WUblastx.64 (Q96L06) Similar to RIKEN cDNA Q96L06 100% 19 717 1700011E04 gene. HTEDY42 519372 898 HMMER PFAM: SCP-like extracellular PF00188 20 −98 −193 2.1.1 protein WUblastx.64 (Q96L06) Similar to RIKEN cDNA Q96L06 100% 33% 19576224 231719700 1700011E04 gene. 94% HTEGI42 908143 555 WUblastx.64 (Q8WW43) Hypothetical 28.5 kDa Q8WW43 99% 26 796 protein. HTEGI42 904624 899 WUblastx.64 (Q8WW43) Hypothetical 28.5 kDa Q8WW43 99% 145 915 protein. HTEGI42 850770 900 WUblastx.64 (AAL93028) Hypothetical 26.9 kDa AAL93028 76% 79% 79% 154154154 263838383 protein. 79% 79% 154154153 825454672 72% 81% 155156155 6238 83% 96% 154154 85% 79% HTEGI42 847564 901 WUblastx.64 (Q14288) HYPOTHETICAL Q14288 92% 61% 503444 4291 PROTEIN (FRAGMENT). HTEHR24 835894 556 WUblastx.64 (Q9HBV2) SPERM MEMBRANE Q9HBV2 76% 84 959 ANTIGEN SMARC32. HTEHR24 513039 903 WUblastx.64 (Q9HBV2) SPERM MEMBRANE Q9HBV2 76% 100% 41692514 529922693 ANTIGEN SMARC32. 96% HTEHU93 722254 557 WUblastx.64 (O60676) CYSTATIN-RELATED CRES_HUMAN 100% 188 613 EPIDIDYMAL SPERMATOGENIC PROTEIN HTEHU93 423009 904 HMMER PFAM: Cystatin domain PF00031 31.7 35 −105 2.1.1 WUblastx.64 (O60676) CYSTATIN-RELATED CRES_HUMAN 100% 78% 504187 614552 EPIDIDYMAL SPERMATOGENIC PROTEIN HTEJN13 1352272 560 WUblastx.64 (Q9BWY1) BA552M11.5 (NOVEL Q9BWY1 100% 100% 158351 193779 PROTEIN) (FRAGMENT). HTEJN13 658744 905 WUblastx.64 (Q9DAR9) 1700001D09RIK Q9DAR9 60% 77% 525163 743516 PROTEIN. HTEJN13 381941 906 WUblastx.64 (Q9HBK8) AD026. Q9HBK8 92% 94% 191214 229633 HTEPG70 834931 562 WUblastx.64 (O75295) R27328_2. O75295 93% 23 268 HTGAU75 597467 563 WUblastx.64 (Q9NZX5) HSPC062. Q9NZX5 55% 72% 502149 672661 HTGEP89 410582 564 WUblastx.64 (Q9DAL9) 1700007K09RIK Q9DAL9 44% 258 566 PROTEIN. HTHBG43 919911 565 WUblastx.64 (Q9NX17) CDNA FLJ20489 FIS, Q9NX17 52% 846 517 CLONE KAT08285. HTHDJ94 693652 567 HMMER PFAM: Oxidoreductase FAD/NAD- PF00175 160.3 552 896 2.1.1 binding domain WUblastx.64 (Q9UHQ9) NADH- Q9UHQ9 89% 66 941 CYTOCHROME B5 REDUCTASE ISOFORM. HTHDS25 772559 568 WUblastx.64 (Q9P1H3) PRO1438. Q9P1H3 66% 1045 911 HTJMA95 706618 569 HMMER PFAM: Ammonium Transporter PF00909 62.1 533 691 2.1.1 Family WUblastx.64 (Q9UBD6) RH TYPE C Q9UBD6 98% 100% 3449 4551069 GLYCOPROTEIN (TUMOR- RELATED PROTEIN DRC2). HTJML75 1040047 570 WUblastx.64 (Q9UJX6) ANAPHASE- Q9UJX6 100% 30 2495 PROMOTING COMPLEX SUBUNIT 2. HTJML75 873355 909 WUblastx.64 (Q9UJX6) ANAPHASE- Q9UJX6 95% 98% 94% 40423911 423101625 PROMOTING COMPLEX 03 SUBUNIT 2. HTLAA40 519329 571 WUblastx.64 (Q9NV11) CDNA FLJ11004 FIS, Q9NV11 100% 100% 36014 482217 CLONE PLACE1002941. HTLBE23 902187 572 WUblastx.64 (Q96M29) CDNA FLJ32871 fis, Q96M29 98% 93% 81% 1768401112 8389801177 clone TESTI2003914, weakly similar to Tek HTLBE23 885431 910 WUblastx.64 (Q96M29) CDNA FLJ32871 fis, Q96M29 92% 796 98 clone TESTI2003914, weakly similar to Tek HTLEP53 634852 573 WUblastx.64 (Q8WTZ3) Hypothetical 27.2 kDa Q8WTZ3 66% 68% 543806 499534 protein. HTLFE42 460583 574 WUblastx.64 (Q9NSI0) PRED58 PROTEIN Q9NSI0 99% 17 346 (FRAGMENT). HTLFE57 1352310 575 WUblastx.64 (Q9D2V1) 2310009N05RIK Q9D2V1 88% 1 687 PROTEIN. HTLFE57 791409 911 WUblastx.64 (Q9D7G6) 2310009N05RIK Q9D7G6 90% 12 698 PROTEIN. HTLFE57 608317 912 WUblastx.64 (Q9D7G6) 2310009N05RIK Q9D7G6 90% 2 619 PROTEIN. HTLGE31 1035130 576 WUblastx.64 (Q9NY64) GLUCOSE Q9NY64 81% 3 149 TRANSPORTER. HTLHY14 838460 577 WUblastx.64 (Q96L02) Hypothetical 24.5 kDa Q96L02 99% 100% 36528 434773 protein. HTLIT32 833906 578 WUblastx.64 (Q96QH1) NB1 Glycoprotein Q96QH1 32% 28% 312330 9321007 precursor. HTLIV19 1046341 579 WUblastx.64 (Q96LS9) CDNA FLJ25101 fis, Q96LS9 50% 69% 119178 172315 clone CBR01328. HTODK73 526021 582 WUblastx.64 (Q9H8P2) CDNA FLJ13348 FIS, Q9H8P2 93% 100% 404567433 448707474 CLONE OVARC1002127, 71% 43% 61% 441821 189519401 WEAKLY SIMILAR TO SOD 80% HTOHM15 1028538 585 WUblastx.64 (Q9NVL9) CDNA FLJ10649 FIS, Q9NVL9 96% 100% 16411507 17181650 CLONE NT2RP2005835, WEAKLY SIMILAR TO SHP HTOHM15 848200 915 HMMER PFAM: UBX domain PF00789 97.6 794 1033 2.1.1 WUblastx.64 (Q9H102) DJ776F14.1 Q9H102 100% 97% 3795 1291036 (ORTHOLOG OF MOUSE P47). HTOHM15 848196 916 WUblastx.64 (Q9NVL9) CDNA FLJ10649 FIS, Q9NVL9 96% 100% 13071173 13841316 CLONE NT2RP2005835, WEAKLY SIMILAR TO SHP HTOIZ02 847904 917 WUblastx.64 ataxin 7 - human pir|T09193|T09193 99% 31% 47% 714437303 119661935 28% 97% 2242 9718736 HTOJA73 797108 589 WUblastx.64 (Q9H387) PRO2550. Q9H387 63% 74% 10441246 9551046 HTOJK60 545067 590 WUblastx.64 (Q9HA67) CDNA FLJ12155 FIS, Q9HA67 73% 78% 745870 644757 CLONE MAMMA1000472. HTPBW79 1317835 591 WUblastx.64 (Q96S93) Hypothetical 41.7 kDa Q96S93 100% 178 1263 protein. HTPBW79 581435 918 WUblastx.64 (Q96S93) Hypothetical 41.7 kDa Q96S93 99% 302 1387 protein. HTPBW79 396459 919 WUblastx.64 (Q9BWS9) UNKNOWN (PROTEIN Q9BWS9 62% 99% 119892 12691243 FOR MGC: 3234). HTTDB46 812763 593 WUblastx.64 (Q9Y2C7) BUTYROPHILIN LIKE Q9Y2C7 70% 83% 59% 106727100 543762107 RECEPTOR. 100% 71644 22180 HTTDB46 909573 920 HMMER PFAM: SPRY domain PF00622 65.9 −956 −1276 2.1.1 HTWCT03 429618 594 WUblastx.64 (O95014) WUGSC: H_DJ0855D21.2 O95014 82% 1488 1592 PROTEIN. HTWDF76 714344 595 WUblastx.64 (Q9BTF2) REC8P, A MEIOTIC Q9BTF2 100% 92% 792370717 875510498 RECOMBINATION AND SISTER 27% 35% 37% 937954217 238525688 CHROMATID COHESION 79% 70% 94 280192 76% HTXAJ12 1310814 596 WUblastx.64 (Q9D7W4) 2210021G21RIK Q9D7W4 45% 57% 1297 77273 PROTEIN. HTXAJ12 567434 921 WUblastx.64 (AAH24685) Similar to AAH24685 100% 98% 997 95267 transmembrane 4 superfamily m HTXDW56 695765 598 WUblastx.64 (Q96A54) Similar to CGI-45 protein Q96A54 99% 7 819 (Hypothetical 42.6 kDa protein). HTXFL30 620001 599 WUblastx.64 (Q96KR5) Leishmanolysin-like Q96KR5 98% 100% 3053021368 199068299 peptidase, variant 2 (EC 3.4.24.36). 100% 100% 94 HTXKF95 891275 600 WUblastx.64 (AAH08360) Similar to hypothetical AAH08360 84% 92% 32481 644203 protein FLJ22376 HTXKF95 834438 923 WUblastx.64 (AAH08360) Similar to hypothetical AAH08360 100% 2 553 protein FLJ22376 HTXKP61 824083 601 WUblastx.64 (Q9H0S8) HYPOTHETICAL 53.0 KDA Q9H0S8 83% 3 1064 PROTEIN. HUDBZ89 1352211 602 WUblastx.64 (Q9VH80) CG16908 PROTEIN. Q9VH80 23% 271 1530 HUDBZ89 562791 924 WUblastx.64 (Q9VH80) CG16908 PROTEIN. Q9VH80 22% 33% 7330 327641 HUFEF62 645101 604 WUblastx.64 hypothetical L1 protein (third intron pir|JU0033|JU0033 81% 84% 355314 30812 of gene TS) - human HUFEF62 630097 926 WUblastx.64 hypothetical L1 protein (third intron pir|JU0033|JU0033 81% 84% 347306 3004 of gene TS) - human HUKAH51 1352424 605 WUblastx.64 (Q96NZ9) Proline-rich acidic Q96NZ9 100% 286 738 protein. HUKAH51 1300737 927 WUblastx.64 (Q96NZ9) Proline-rich acidic Q96NZ9 94% 144 569 protein. HUKAH51 603538 928 WUblastx.64 (Q96NZ9) Proline-rich acidic Q96NZ9 100% 93% 46255 479462 protein. HUKBT29 694590 606 WUblastx.64 (Q96AA2) Obscurin. Q96AA2 82% 30% 33% 131520500 130059757 29% 10% 152103959 137013387 34% 28% 7134 10316 HUSIG64 566762 607 WUblastx.64 (O60763) GENERAL VESICULAR VDP_HUMAN 100% 9 977 TRANSPORT FACTOR P115 (TRANSCYTO HUSXS50 1352367 608 WUblastx.64 (Q9Y311) F-BOX ONLY PROTEIN FBX7_HUMAN 100% 280 1845 7. HUSXS50 883176 929 WUblastx.64 (AAH08361) F-box only protein 7. AAH08361 99% 42% 100% 281156610 106916221 67 666 HUSXS50 655372 930 WUblastx.64 (AAH08361) F-box only protein 7. AAH08361 77% 26% 100% 143317 459219700 HVARW53 1194812 609 WUblastx.64 (Q9V6L4) CG12251 PROTEIN. Q9V6L4 38% 24% 62387 748620 HVARW53 1044491 931 WUblastx.64 (Q9V6L4) CG12251 PROTEIN. Q9V6L4 40% 25% 56972 673581 HWAAD63 838626 610 HMMER PFAM: Sodium/calcium exchanger PF01699 62.8 346 453 2.1.1 protein WUblastx.64 (Q9HC58) SODIUM/CALCIUM Q9HC58 65% 229 813 EXCHANGER NCKX3. HWAAD63 833089 932 HMMER PFAM: Sodium/calcium exchanger PF01699 37.8 346 453 2.1.1 protein WUblastx.64 (Q9HC58) SODIUM/CALCIUM Q9HC58 78% 55% 72% 229429533 453596814 EXCHANGER NCKX3. HWAAD63 793875 933 HMMER PFAM: Sodium/calcium exchanger PF01699 113.7 336 773 2.1.1 protein WUblastx.64 (Q9HC58) SODIUM/CALCIUM Q9HC58 76% 219 806 EXCHANGER NCKX3. HWABY10 768334 612 WUblastx.64 (Q96AW1) Hypothetical 19.2 kDa Q96AW1 100% 165 665 protein. HWBAO62 838164 614 HMMER PFAM: Immunoglobulin domain PF00047 27.9 202 402 2.1.1 WUblastx.64 (Q14288) HYPOTHETICAL Q14288 45% 66% 62% 133111581 161813341 PROTEIN (FRAGMENT). 55% 8471594 8941839 HWBAO62 625914 934 WUblastx.64 (Q14288) HYPOTHETICAL Q14288 43% 62% 66% 135818741 164519211 PROTEIN (FRAGMENT). 55% 1851621 3611866 HWBAR88 836469 615 WUblastx.64 (Q9Y2C2) Q9Y2C2 96% 100% 215107958 9822411050 DERMATAN/CHONDROITIN 83% SULFATE 2- SULFOTRANSFERASE. HWBCB89 1093347 616 WUblastx.64 (BAB55294) CDNA FLJ14777 fis, BAB55294 100% 37 597 clone NT2RP4000259, w HWBCB89 886210 935 HMMER PFAM: Glutathione peroxidases PF00255 170.2 104 433 2.1.1 WUblastx.64 (BAB55294) CDNA FLJ14777 fis, BAB55294 100% 35 595 clone NT2RP4000259, w HWBCP79 846382 617 WUblastx.64 (Q96MM0) CDNA FLJ32172 fis, Q96MM0 27% 85% 340158 14378 clone PLACE6000555. HWBCP79 646977 936 WUblastx.64 (Q96MM0) CDNA FLJ32172 fis, Q96MM0 27% 85% 330148 13368 clone PLACE6000555. HWBDP28 1352265 618 WUblastx.64 (Q9H687) CDNA: FLJ22494 FIS, Q9H687 99% 480 1079 CLONE HRC11131. HWBFE57 907063 619 WUblastx.64 (Q9NR73) MACROPHAGE ABC Q9NR73 93% 206 1048 TRANSPORTER. HWBFE57 907067 938 WUblastx.64 (Q96S58) ABCA-SSN. Q96S58 99% 50% 97% 278495258 196905513 29% 47% 014499455 341344500 29% 29% 052837275 109358749 29% 37% 062412332 073362303 32% 37% 741293215 853220034 36% 52% 250142545 964123513 31% 29% 233488144 245612783 20% 94% 6251692049 44231708 97% 20% HWBFE57 876136 939 WUblastx.64 (Q14287) HYPOTHETICAL Q14287 58% 252 13 PROTEIN (FRAGMENT). HWDAH38 1028519 621 WUblastx.64 (Q9NX85) CDNA FLJ20378 FIS, Q9NX85 71% 69% 48% 943111316 111912501 CLONE KAIA0536. 00 340 HWDAH38 889281 941 WUblastx.64 (Q64150) NUCLEAR Q64150 60% 795 673 LOCALIZATION SIGNAL BINDING PROTEIN. HWHGP71 995431 622 HMMER PFAM: 7 transmembrane receptor PF00001 31.2 389 766 2.1.1 (rhodopsin family) WUblastx.64 leukotriene B4 receptor 2, BLTR2 - pir|JC7356|JC7356 56% 47% 74% 766434101 1020484766 human HWHGP71 839250 942 blastx.2 (AJ278605) leukotriene B4 receptor emb|CAB96134.1| 77% 100% 106555776 4657701036 2 [Homo sapiens] 58% HWHGQ49 1352257 623 WUblastx.64 (AAH25278) Androgen induced AAH25278 100% 26 706 protein. HWHGQ49 636080 943 WUblastx.64 (AAH25278) Androgen induced AAH25278 93% 42 725 protein. HWHGU54 695695 624 HMMER PFAM: Serpins (serine protease PF00079 501.1 277 1377 2.1.1 inhibitors) WUblastx.64 (AAL99574) OL-64 protein. AAL99574 62% 145 1377 HWHGZ51 886212 625 WUblastx.64 (Q9UJ74) HYPOTHETICAL 36.0 KDA Q9UJ74 100% 33 1070 PROTEIN (C4.4A PROTEIN). HWHHL34 805642 626 WUblastx.64 (O75915) JWA PROTEIN O75915 100% 131 694 (HSPC127) (VITAMIN A RESPONSIVE, CYTOSKELETON RE HWHHL34 801943 944 WUblastx.64 (O75915) JWA PROTEIN O75915 92% 53 613 (HSPC127) (VITAMIN A RESPONSIVE, CYTOSKELETON RE HWHHL34 341560 945 WUblastx.64 (O75915) JWA PROTEIN O75915 100% 101 664 (HSPC127) (VITAMIN A RESPONSIVE, CYTOSKELETON RE HWLEV32 1032602 627 WUblastx.64 (O00378) PUTATIVE P150. O00378 44% 38% 684556 53517 HWLEV32 873296 946 WUblastx.64 retrovirus-related reverse pir|A25313|GNHUL1 50% 40% 614510 5257 transcriptase pseudogene - human HWLEV32 881710 947 WUblastx.64 (BAB85074) CDNA FLJ23835 fis, BAB85074 97% 61 396 clone KAIA2214. HWLEV32 846351 948 WUblastx.64 (BAB85074) CDNA FLJ23835 fis, BAB85074 99% 2 409 clone KAIA2214. HWLIH65 793713 628 HMMER PFAM: Integral membrane protein PF01940 49.3 147 455 2.1.1 WUblastx.64 (AAH08596) Unknown (protein for AAH08596 98% 81 623 MGC: 16985). HYAAJ71 826754 630 WUblastx.64 (Q9NX17) CDNA FLJ20489 FIS, Q9NX17 62% 1147 1464 CLONE KAT08285. HUSBA88 895435 631 HMMER PFAM: Glycosyl hydrolase family PF01532 694 783 2102 2.1.1 47 WUblastx.64 (Q9UKM7) ALPHA 1,2- Q9UKM7 94% 18 2114 MANNOSIDASE.

Race Protocol for Recovery of Full-Length Genes

Partial cDNA clones can be made full-length by utilizing the rapid amplification of cDNA ends (RACE) procedure described in Frohman, M. A., et al., Proc. Nat'l. Acad. Sci. USA, 85:8998-9002 (1988). A cDNA clone missing either the 5′ or 3′ end can be reconstructed to include the absent base pairs extending to the translational start or stop codon, respectively. In some cases, cDNAs are missing the start codon of translation, therefor. The following briefly describes a modification of this original 5′ RACE procedure. Poly A+ or total RNA is reverse transcribed with Superscript II (Gibco/BRL) and an antisense or complementary primer specific to the cDNA sequence. The primer is removed from the reaction with a Microcon Concentrator (Amicon). The first-strand cDNA is then tailed with dATP and terminal deoxynucleotide transferase (Gibco/BRL). Thus, an anchor sequence is produced which is needed for PCR amplification. The second strand is synthesized from the dA-tail in PCR buffer, Taq DNA polymerase (Perkin-Elmer Cetus), an oligo-dT primer containing three adjacent restriction sites (XhoI, SalI and ClaI) at the 5′ end and a primer containing just these restriction sites. This double-stranded cDNA is PCR amplified for 40 cycles with the same primers as well as a nested cDNA-specific antisense primer. The PCR products are size-separated on an ethidium bromide-agarose gel and the region of gel containing cDNA products the predicted size of missing protein-coding DNA is removed. cDNA is purified from the agarose with the Magic PCR Prep kit (PROMEGA™), restriction digested with XhoI or SalI, and ligated to a plasmid such as pBLUESCRIPT™ SKII (STRATAGENE™) at XhoI and EcoRV sites. This DNA is transformed into bacteria and the plasmid clones sequenced to identify the correct protein-coding inserts. Correct 5′ ends are confirmed by comparing this sequence with the putatively identified homologue and overlap with the partial cDNA clone. Similar methods known in the art and/or commercial kits are used to amplify and recover 3′ ends.

Several quality-controlled kits are commercially available for purchase. Similar reagents and methods to those above are supplied in kit form from Gibco/BRL for both 5′ and 3′ RACE for recovery of full length genes. A second kit is available from CLONTECH™ which is a modification of a related technique, SLIC (single-stranded ligation to single-stranded cDNA), developed by Dumas et al., Nucleic Acids Res., 19:5227-32 (1991). The major differences in procedure are that the RNA is alkaline hydrolyzed after reverse transcription and RNA ligase is used to join a restriction site-containing anchor primer to the first-strand cDNA. This obviates the necessity for the dA-tailing reaction which results in a polyT stretch that is difficult to sequence past.

An alternative to generating 5′ or 3′ cDNA from RNA is to use cDNA library double-stranded DNA. An asymmetric PCR-amplified antisense cDNA strand is synthesized with an antisense cDNA-specific primer and a plasmid-anchored primer. These primers are removed and a symmetric PCR reaction is performed with a nested cDNA-specific antisense primer and the plasmid-anchored primer.

RNA Ligase Protocol for Generating the 5′ or 3′ End Sequences to Obtain Full Length Genes

Once a gene of interest is identified, several methods are available for the identification of the 5′ or 3′ portions of the gene which may not be present in the original cDNA plasmid. These methods include, but are not limited to, filter probing, clone enrichment using specific probes and protocols similar and identical to 5′ and 3′ RACE. While the full length gene may be present in the library and can be identified by probing, a useful method for generating the 5′ or 3′ end is to use the existing sequence information from the original cDNA to generate the missing information. A method similar to 5′ RACE is available for generating the missing 5′ end of a desired full-length gene. (This method was published by Fromont-Racine et al., Nucleic Acids Res., 21(7):1683-1684 (1993)). Briefly, a specific RNA oligonucleotide is ligated to the 5′ ends of a population of RNA presumably containing full-length gene RNA transcript and a primer set containing a primer specific to the ligated RNA oligonucleotide and a primer specific to a known sequence of the gene of interest, is used to PCR amplify the 5′ portion of the desired full length gene which may then be sequenced and used to generate the full length gene. This method starts with total RNA isolated from the desired source, poly A RNA may be used but is not a prerequisite for this procedure. The RNA preparation may then be treated with phosphatase if necessary to eliminate 5′ phosphate groups on degraded or damaged RNA which may interfere with the later RNA ligase step. The phosphatase if used is then inactivated and the RNA is treated with tobacco acid pyrophosphatase in order to remove the cap structure present at the 5′ ends of messenger RNAs. This reaction leaves a 5′ phosphate group at the 5′ end of the cap cleaved RNA which can then be ligated to an RNA oligonucleotide using T4 RNA ligase. This modified RNA preparation can then be used as a template for first strand cDNA synthesis using a gene specific oligonucleotide. The first strand synthesis reaction can then be used as a template for PCR amplification of the desired 5′ end using a primer specific to the ligated RNA oligonucleotide and a primer specific to the known sequence of the gene of interest. The resultant product is then sequenced and analyzed to confirm that the 5′ end sequence belongs to the relevant gene.

The present invention also relates to vectors or plasmids which include such DNA sequences, as well as the use of the DNA sequences. The material deposited with the ATCC™ (e.g., as described in columns 2 and 3 of Table 1A, and/or as set forth in Table 1B, Table 6, or Table 7) is a mixture of cDNA clones derived from a variety of human tissue and cloned in either a plasmid vector or a phage vector, as described, for example, in Table 1A and Table 7. These deposits are referred to as “the deposits” herein. The tissues from which some of the clones were derived are listed in Table 7, and the vector in which the corresponding cDNA is contained is also indicated in Table 7. The deposited material includes cDNA clones corresponding to SEQ ID NO:X described, for example, in Table 1A and/or Table 1B (ATCC™ Deposit No:Z). A clone which is isolatable from the ATCC™ Deposits by use of a sequence listed as SEQ ID NO:X, may include the entire coding region of a human gene or in other cases such clone may include a substantial portion of the coding region of a human gene. Furthermore, although the sequence listing may in some instances list only a portion of the DNA sequence in a clone included in the ATCC™ Deposits, it is well within the ability of one skilled in the art to sequence the DNA included in a clone contained in the ATCC™ Deposits by use of a sequence (or portion thereof) described in, for example Tables 1A and/or Table 1B or Table 2, by procedures hereinafter further described, and others apparent to those skilled in the art.

Also provided in Table 1A and Table 7 is the name of the vector which contains the cDNA clone. Each vector is routinely used in the art. The following additional information is provided for convenience.

Vectors Lambda Zap (U.S. Pat. Nos. 5,128,256 and 5,286,636), Uni-Zap XR (U.S. Pat. Nos. 5,128,256 and 5,286,636), Zap Express (U.S. Pat. Nos. 5,128,256 and 5,286,636), pBLUESCRIPT™ (pBS) (Short, J. M. et al., Nucleic Acids Res. 16:7583-7600 (1988); Alting-Mees, M. A. and Short, J. M., Nucleic Acids Res. 17.9494 (1989)) and pBK (Alting-Mees, M. A. et al., Strategies 5:58-61 (1992)) are commercially available from STRATAGENE™ Cloning Systems, Inc., 11011 N. Torrey Pines Road, La Jolla, Calif., 92037. pBS contains an ampicillin resistance gene and pBK contains a neomycin resistance gene. Phagemid pBS may be excised from the Lambda Zap and Uni-Zap XR vectors, and phagemid pBK may be excised from the Zap Express vector. Both phagemids may be transformed into E. coli strain XL-1 Blue, also available from STRATAGENE™.

Vectors pSport1, pCMVSport 1.0, pCMVSport 2.0 and pCMVSport 3.0, were obtained from LIFE TECHNOLOGIES™, Inc., P.O. Box 6009, Gaithersburg, Md. 20897. All Sport vectors contain an ampicillin resistance gene and may be transformed into E. coli strain DH10B, also available from LIFE TECHNOLOGIES™. See, for instance, Gruber, C. E., et al., Focus 15:59-(1993). Vector lafmid BA (Bento Soares, Columbia University, New York, N.Y.) contains an ampicillin resistance gene and can be transformed into E. coli strain XL-1 Blue. Vector pCR®2.1, which is available from Invitrogen, 1600 Faraday Avenue, Carlsbad, Calif. 92008, contains an ampicillin resistance gene and may be transformed into E. coli strain DH10B, available from LIFE TECHNOLOGIES™. See, for instance, Clark, J. M., Nuc. Acids Res. 16:9677-9686 (1988) and Mead, D. et al., Bio/Technology 9: (1991).

The present invention also relates to the genes corresponding to SEQ ID NO:X, SEQ ID NO:Y, and/or the deposited clone (ATCC™ Deposit No:Z). The corresponding gene can be isolated in accordance with known methods using the sequence information disclosed herein. Such methods include preparing probes or primers from the disclosed sequence and identifying or amplifying the corresponding gene from appropriate sources of genomic material.

Also provided in the present invention are allelic variants, orthologs, and/or species homologs. Procedures known in the art can be used to obtain full-length genes, allelic variants, splice variants, full-length coding portions, orthologs, and/or species homologs of genes corresponding to SEQ ID NO:X or the complement thereof, polypeptides encoded by genes corresponding to SEQ ID NO:X or the complement thereof, and/or the cDNA contained in ATCC™ Deposit No:Z, using information from the sequences disclosed herein or the clones deposited with the ATCC™. For example, allelic variants and/or species homologs may be isolated and identified by making suitable probes or primers from the sequences provided herein and screening a suitable nucleic acid source for allelic variants and/or the desired homologue.

The polypeptides of the invention can be prepared in any suitable manner. Such polypeptides include isolated naturally occurring polypeptides, recombinantly produced polypeptides, synthetically produced polypeptides, or polypeptides produced by a combination of these methods. Means for preparing such polypeptides are well understood in the art.

The polypeptides may be in the form of the secreted protein, including the mature form, or may be a part of a larger protein, such as a fusion protein (see below). It is often advantageous to include an additional amino acid sequence which contains secretory or leader sequences, pro-sequences, sequences which aid in purification, such as multiple histidine residues, or an additional sequence for stability during recombinant production.

The polypeptides of the present invention are preferably provided in an isolated form, and preferably are substantially purified. A recombinantly produced version of a polypeptide, including the secreted polypeptide, can be substantially purified using techniques described herein or otherwise known in the art, such as, for example, by the one-step method described in Smith and Johnson, Gene 67:31-40 (1988). Polypeptides of the invention also can be purified from natural, synthetic or recombinant sources using techniques described herein or otherwise known in the art, such as, for example, antibodies of the invention raised against the polypeptides of the present invention in methods which are well known in the art.

The present invention provides a polynucleotide comprising, or alternatively consisting of, the nucleic acid sequence of SEQ ID NO:X, and/or the cDNA sequence contained in ATCC™ Deposit No:Z.

The present invention also provides a polypeptide comprising, or alternatively, consisting of, the polypeptide sequence of SEQ ID NO:Y, a polypeptide encoded by SEQ ID NO:X or a complement thereof, a polypeptide encoded by the cDNA contained in ATCC™ Deposit No:Z, and/or the polypeptide sequence encoded by a nucleotide sequence in SEQ ID NO:B as defined in column 6 of Table 1C. Polynucleotides encoding a polypeptide comprising, or alternatively consisting of the polypeptide sequence of SEQ ID NO:Y, a polypeptide encoded by SEQ ID NO:X, a polypeptide encoded by the cDNA contained in ATCC™ Deposit No:Z, and/or a polypeptide sequence encoded by a nucleotide sequence in SEQ ID NO:B as defined in column 6 of Table 1C are also encompassed by the invention. The present invention further encompasses a polynucleotide comprising, or alternatively consisting of, the complement of the nucleic acid sequence of SEQ ID NO:X, a nucleic acid sequence encoding a polypeptide encoded by the complement of the nucleic acid sequence of SEQ ID NO:X, and/or the cDNA contained in ATCC™ Deposit No:Z.

Moreover, representative examples of polynucleotides of the invention comprise, or alternatively consist of, one, two, three, four, five, six, seven, eight, nine, ten, or more of the sequences delineated in Table 1C column 6, or any combination thereof. Additional, representative examples of polynucleotides of the invention comprise, or alternatively consist of, one, two, three, four, five, six, seven, eight, nine, ten, or more of the complementary strand(s) of the sequences delineated in Table 1C column 6, or any combination thereof. In further embodiments, the above-described polynucleotides of the invention comprise, or alternatively consist of, sequences delineated in Table 1C, column 6, and have a nucleic acid sequence which is different from that of the BAC fragment having the sequence disclosed in SEQ ID NO:B (see Table 1C, column 5). In additional embodiments, the above-described polynucleotides of the invention comprise, or alternatively consist of, sequences delineated in Table 1C, column 6, and have a nucleic acid sequence which is different from that published for the BAC clone identified as BAC ID NO:A (see Table 1C, column 4). In additional embodiments, the above-described polynucleotides of the invention comprise, or alternatively consist of, sequences delineated in Table 1C, column 6, and have a nucleic acid sequence which is different from that contained in the BAC clone identified as BAC ID NO:A (see Table 1C, column 4). Polypeptides encoded by these polynucleotides, other polynucleotides that encode these polypeptides, and antibodies that bind these polypeptides are also encompassed by the invention. Additionally, fragments and variants of the above-described polynucleotides and polypeptides are also encompassed by the invention.

Further, representative examples of polynucleotides of the invention comprise, or alternatively consist of, one, two, three, four, five, six, seven, eight, nine, ten, or more of the sequences delineated in column 6 of Table 1C which correspond to the same Clone ID (see Table 1C, column 1), or any combination thereof. Additional, representative examples of polynucleotides of the invention comprise, or alternatively consist of, one, two, three, four, five, six, seven, eight, nine, ten, or more of the complementary strand(s) of the sequences delineated in column 6 of Table 1C which correspond to the same Clone ID (see Table 1C, column 1), or any combination thereof. In further embodiments, the above-described polynucleotides of the invention comprise, or alternatively consist of, sequences delineated in column 6 of Table 1C which correspond to the same Clone ID (see Table 1C, column 1) and have a nucleic acid sequence which is different from that of the BAC fragment having the sequence disclosed in SEQ ID NO:B (see Table 1C, column 5). In additional embodiments, the above-described polynucleotides of the invention comprise, or alternatively consist of, sequences delineated in column 6 of Table 1C which correspond to the same Clone ID (see Table 1C, column 1) and have a nucleic acid sequence which is different from that published for the BAC clone identified as BAC ID NO:A (see Table 1C, column 4). In additional embodiments, the above-described polynucleotides of the invention comprise, or alternatively consist of, sequences delineated in column 6 of Table 1C which correspond to the same Clone ID (see Table 1C, column 1) and have a nucleic acid sequence which is different from that contained in the BAC clone identified as BAC ID NO:A (see Table 1C, column 4). Polypeptides encoded by these polynucleotides, other polynucleotides that encode these polypeptides, and antibodies that bind these polypeptides are also encompassed by the invention. Additionally, fragments and variants of the above-described polynucleotides and polypeptides are also encompassed by the invention.

Further, representative examples of polynucleotides of the invention comprise, or alternatively consist of, one, two, three, four, five, six, seven, eight, nine, ten, or more of the sequences delineated in column 6 of Table 1C which correspond to the same contig sequence identifier SEQ ID NO:X (see Table 1C, column 2), or any combination thereof. Additional, representative examples of polynucleotides of the invention comprise, or alternatively consist of, one, two, three, four, five, six, seven, eight, nine, ten, or more of the complementary strand(s) of the sequences delineated in column 6 of Table 1C which correspond to the same contig sequence identifier SEQ ID NO:X (see Table 1C, column 2), or any combination thereof. In further embodiments, the above-described polynucleotides of the invention comprise, or alternatively consist of, sequences delineated in column 6 of Table 1C which correspond to the same contig sequence identifier SEQ ID NO:X (see Table 1C, column 2) and have a nucleic acid sequence which is different from that of the BAC fragment having the sequence disclosed in SEQ ID NO:B (see Table 1C, column 5). In additional embodiments, the above-described polynucleotides of the invention comprise, or alternatively consist of, sequences delineated in column 6 of Table 1C which correspond to the same contig sequence identifier SEQ ID NO:X (see Table 1C, column 2) and have a nucleic acid sequence which is different from that published for the BAC clone identified as BAC ID NO:A (see Table 1C, column 4). In additional embodiments, the above-described polynucleotides of the invention comprise, or alternatively consist of, sequences delineated in column 6 of Table 1C which correspond to the same contig sequence identifier SEQ ID NO:X (see Table 1C, column 2) and have a nucleic acid sequence which is different from that contained in the BAC clone identified as BAC ID NO:A (See Table 1C, column 4). Polypeptides encoded by these polynucleotides, other polynucleotides that encode these polypeptides, and antibodies that bind these polypeptides are also encompassed by the invention. Additionally, fragments and variants of the above-described polynucleotides and polypeptides are also encompassed by the invention.

Moreover, representative examples of polynucleotides of the invention comprise, or alternatively consist of, one, two, three, four, five, six, seven, eight, nine, ten, or more of the sequences delineated in the same row of Table 1C column 6, or any combination thereof. Additional, representative examples of polynucleotides of the invention comprise, or alternatively consist of, one, two, three, four, five, six, seven, eight, nine, ten, or more of the complementary strand(s) of the sequences delineated in the same row of Table 1C column 6, or any combination thereof. In preferred embodiments, the polynucleotides of the invention comprise, or alternatively consist of, one, two, three, four, five, six, seven, eight, nine, ten, or more of the complementary strand(s) of the sequences delineated in the same row of Table 1C column 6, wherein sequentially delineated sequences in the table (i.e. corresponding to those exons located closest to each other) are directly contiguous in a 5′ to 3′ orientation. In further embodiments, above-described polynucleotides of the invention comprise, or alternatively consist of, sequences delineated in the same row of Table 1C, column 6, and have a nucleic acid sequence which is different from that of the BAC fragment having the sequence disclosed in SEQ ID NO:B (see Table 1C, column 5). In additional embodiments, the above-described polynucleotides of the invention comprise, or alternatively consist of, sequences delineated in the same row of Table 1C, column 6, and have a nucleic acid sequence which is different from that published for the BAC clone identified as BAC ID NO:A (see Table 1C, column 4). In additional embodiments, the above-described polynucleotides of the invention comprise, or alternatively consist of, sequences delineated in the same row of Table 1C, column 6, and have a nucleic acid sequence which is different from that contained in the BAC clone identified as BAC ID NO:A (see Table 1C, column 4). Polypeptides encoded by these polynucleotides, other polynucleotides that encode these polypeptides, and antibodies that bind these polypeptides are also encompassed by the invention.

In additional specific embodiments, polynucleotides of the invention comprise, or alternatively consist of, one, two, three, four, five, six, seven, eight, nine, ten, or more of the sequences delineated in column 6 of Table 1C, and the polynucleotide sequence of SEQ ID NO:X (e.g., as defined in Table 1C, column 2) or fragments or variants thereof. Polypeptides encoded by these polynucleotides, other polynucleotides that encode these polypeptides, and antibodies that bind these polypeptides are also encompassed by the invention.

In additional specific embodiments, polynucleotides of the invention comprise, or alternatively consist of, one, two, three, four, five, six, seven, eight, nine, ten, or more of the sequences delineated in column 6 of Table 1C which correspond to the same Clone ID (see Table 1C, column 1), and the polynucleotide sequence of SEQ ID NO:X (e.g., as defined in Table 1A, Table 1B, or Table 1C) or fragments or variants thereof. In preferred embodiments, the delineated sequence(s) and polynucleotide sequence of SEQ ID NO:X correspond to the same Clone ID. Polypeptides encoded by these polynucleotides, other polynucleotides that encode these polypeptides, and antibodies that bind these polypeptides are also encompassed by the invention.

In further specific embodiments, polynucleotides of the invention comprise, or alternatively consist of, one, two, three, four, five, six, seven, eight, nine, ten, or more of the sequences delineated in the same row of column 6 of Table 1C, and the polynucleotide sequence of SEQ ID NO:X (e.g., as defined in Table 1A, Table 1B, or Table 1C) or fragments or variants thereof. In preferred embodiments, the delineated sequence(s) and polynucleotide sequence of SEQ ID NO:X correspond to the same row of column 6 of Table 1C. Polypeptides encoded by these polynucleotides, other polynucleotides that encode these polypeptides, and antibodies that bind these polypeptides are also encompassed by the invention.

In additional specific embodiments, polynucleotides of the invention comprise, or alternatively consist of a polynucleotide sequence in which the 3′ 10 polynucleotides of one of the sequences delineated in column 6 of Table 1C and the 5′ 10 polynucleotides of the sequence of SEQ ID NO:X are directly contiguous. Nucleic acids which hybridize to the complement of these 20 contiguous polynucleotides under stringent hybridization conditions or alternatively, under lower stringency conditions, are also encompassed by the invention. Polypeptides encoded by these polynucleotides and/or nucleic acids, other polynucleotides and/or nucleic acids that encode these polypeptides, and antibodies that bind these polypeptides are also encompassed by the invention. Additionally, fragments and variants of the above-described polynucleotides, nucleic acids, and polypeptides are also encompassed by the invention.

In additional specific embodiments, polynucleotides of the invention comprise, or alternatively consist of, a polynucleotide sequence in which the 3′ 10 polynucleotides of one of the sequences delineated in column 6 of Table 1C and the 5′ 10 polynucleotides of a fragment or variant of the sequence of SEQ ID NO:X are directly contiguous Nucleic acids which hybridize to the complement of these 20 contiguous polynucleotides under stringent hybridization conditions or alternatively, under lower stringency conditions, are also encompassed by the invention. Polypeptides encoded by these polynucleotides and/or nucleic acids, other polynucleotides and/or nucleic acids encoding these polypeptides, and antibodies that bind these polypeptides are also encompassed by the invention. Additionally, fragments and variants of the above-described polynucleotides, nucleic acids, and polypeptides are also encompassed by the invention.

In specific embodiments, polynucleotides of the invention comprise, or alternatively consist of, a polynucleotide sequence in which the 3′ 10 polynucleotides of the sequence of SEQ ID NO:X and the 5′ 10 polynucleotides of the sequence of one of the sequences delineated in column 6 of Table 1C are directly contiguous. Nucleic acids which hybridize to the complement of these 20 contiguous polynucleotides under stringent hybridization conditions or alternatively, under lower stringency conditions, are also encompassed by the invention. Polypeptides encoded by these polynucleotides and/or nucleic acids, other polynucleotides and/or nucleic acids encoding these polypeptides, and antibodies that bind these polypeptides are also encompassed by the invention. Additionally, fragments and variants of the above-described polynucleotides, nucleic acids, and polypeptides are also encompassed by the invention.

In specific embodiments, polynucleotides of the invention comprise, or alternatively consist of, a polynucleotide sequence in which the 3′ 10 polynucleotides of a fragment or variant of the sequence of SEQ ID NO:X and the 5′ 10 polynucleotides of the sequence of one of the sequences delineated in column 6 of Table 1C are directly contiguous. Nucleic acids which hybridize to the complement of these 20 contiguous polynucleotides under stringent hybridization conditions or alternatively, under lower stringency conditions, are also encompassed by the invention. Polypeptides encoded by these polynucleotides and/or nucleic acids, other polynucleotides and/or nucleic acids encoding these polypeptides, and antibodies that bind these polypeptides are also encompassed by the invention. Additionally, fragments and variants of the above-described polynucleotides, nucleic acids, and polypeptides, are also encompassed by the invention.

In further specific embodiments, polynucleotides of the invention comprise, or alternatively consist of, a polynucleotide sequence in which the 3′ 10 polynucleotides of one of the sequences delineated in column 6 of Table 1C and the 5′ 10 polynucleotides of another sequence in column 6 are directly contiguous. Nucleic acids which hybridize to the complement of these 20 contiguous polynucleotides under stringent hybridization conditions or alternatively, under lower stringency conditions, are also encompassed by the invention. Polypeptides encoded by these polynucleotides and/or nucleic acids, other polynucleotides and/or nucleic acids encoding these polypeptides, and antibodies that bind these polypeptides are also encompassed by the invention. Additionally, fragments and variants of the above-described polynucleotides, nucleic acids, and polypeptides are also encompassed by the invention.

In specific embodiments, polynucleotides of the invention comprise, or alternatively consist of, a polynucleotide sequence in which the 3′ 10 polynucleotides of one of the sequences delineated in column 6 of Table 1C and the 5′ 10 polynucleotides of another sequence in column 6 corresponding to the same Clone ID (see Table 1C, column 1) are directly contiguous. Nucleic acids which hybridize to the complement of these 20 lower stringency conditions, are also encompassed by the invention. Polypeptides encoded by these polynucleotides and/or nucleic acids, other polynucleotides and/or nucleic acids encoding these polypeptides, and antibodies that bind these polypeptides are also encompassed by the invention. Additionally, fragments and variants of the above-described polynucleotides, nucleic acids, and polypeptides are also encompassed by the invention.

In specific embodiments, polynucleotides of the invention comprise, or alternatively consist of, a polynucleotide sequence in which the 3′ 10 polynucleotides of one sequence in column 6 corresponding to the same contig sequence identifier SEQ ID NO:X (see Table 1C, column 2) are directly contiguous. Nucleic acids which hybridize to the complement of these 20 contiguous polynucleotides under stringent hybridization conditions or alternatively, under lower stringency conditions, are also encompassed by the invention. Polypeptides encoded by these polynucleotides and/or nucleic acids, other polynucleotides and/or nucleic acids encoding these polypeptides, and antibodies that bind these polypeptides are also encompassed by the invention. Additionally, fragments and variants of the above-described polynucleotides, nucleic acids, and polypeptides are also encompassed by the invention.

In specific embodiments, polynucleotides of the invention comprise, or alternatively consist of a polynucleotide sequence in which the 3′ 10 polynucleotides of one of the sequences delineated in column 6 of Table 1C and the 5′ 10 polynucleotides of another sequence in column 6 corresponding to the same row are directly contiguous. In preferred embodiments, the 3′ 10 polynucleotides of one of the sequences delineated in column 6 of Table 1C is directly contiguous with the 5′ 10 polynucleotides of the next sequential exon delineated in Table 1C, column 6. Nucleic acids which hybridize to the complement of these 20 contiguous polynucleotides under stringent hybridization conditions or alternatively, under lower stringency conditions, are also encompassed by the invention. Polypeptides encoded by these polynucleotides and/or nucleic acids, other polynucleotides and/or nucleic acids encoding these polypeptides, and antibodies that bind these polypeptides are also encompassed by the invention. Additionally, fragments and variants of the above-described polynucleotides, nucleic acids, and polypeptides are also encompassed by the invention.

Table 3

Many polynucleotide sequences, such as EST sequences, are publicly available and accessible through sequence databases and may have been publicly available prior to conception of the present invention. Preferably, such related polynucleotides are specifically excluded from the scope of the present invention. Accordingly, for each contig sequence (SEQ ID NO:X) listed in the fifth column of Table 1A and/or the fourth column of Table 1B, preferably excluded are one or more polynucleotides comprising a nucleotide sequence described by the general formula of a-b, where a is any integer between 1 and the final nucleotide minus 15 of SEQ ID NO:X, b is an integer of 15 to the final nucleotide of SEQ ID NO:X, where both a and b correspond to the positions of nucleotide residues shown in SEQ ID NO:X, and where b is greater than or equal to a+14. More specifically, preferably excluded are one or more polynucleotides comprising a nucleotide sequence described by the general formula of a-b, where a and b are integers as defined in columns 4 and 5, respectively, of Table 3. In specific embodiments, the polynucleotides of the invention do not consist of at least one, two, three, four, five, ten, or more of the specific polynucleotide sequences referenced by the Genbank Accession No. as disclosed in column 6 of Table 3 (including for example, published sequence in connection with a particular BAC clone). In further embodiments, preferably excluded from the invention are the specific polynucleotide sequence(s) contained in the clones corresponding to at least one, two, three, four, five, ten, or more of the available material having the accession numbers identified in the sixth column of this Table (including for example, the actual sequence contained in an identified BAC clone). In no way is this listing meant to encompass all of the sequences which may be excluded by the general formula, it is just a representative example. All references available through these accessions are hereby incorporated by reference in their entirety. LENGTHY TABLE REFERENCED HERE US20080103090A1-20080501-T00004 Please refer to the end of the specification for access instructions.

Description of Table 4

Table 4 provides a key to the tissue/cell source identifier code disclosed in Table 1B.2, column 5. Column 1 of Table 4 provides the tissue/cell source identifier code disclosed in Table 1B.2, Column 5. Columns 2-5 provide a description of the tissue or cell source. Note that “Description” and “Tissue” sources (i.e. columns 2 and 3) having the prefix “a_” indicates organs, tissues, or cells derived from “adult” sources. Codes corresponding to diseased tissues are indicated in column 6 with the word “disease.” The use of the word “disease” in column 6 is non-limiting. The tissue or cell source may be specific (e.g. a neoplasm), or may be disease-associated (e.g., a tissue sample from a normal portion of a diseased organ). Furthermore, tissues and/or cells lacking the “disease” designation may still be derived from sources directly or indirectly involved in a disease state or disorder, and therefore may have a further utility in that disease state or disorder. In numerous cases where the tissue/cell source is a library, column 7 identifies the vector use d to generate the library. TABLE 4 Code Description Tissue Organ Cell Line Disease Vector AR022 a_Heart a_Heart AR023 a_Liver a_Liver AR024 a_mammary gland a_mammary gland AR025 a_Prostate a_Prostate AR026 a_small intestine a_small intestine AR027 a_Stomach a_Stomach AR028 Blood B cells Blood B cells AR029 Blood B cells activated Blood B cells activated AR030 Blood B cells resting Blood B cells resting AR031 Blood T cells activated Blood T cells activated AR032 Blood T cells resting Blood T cells resting AR033 brain brain AR034 breast breast AR035 breast cancer breast cancer AR036 Cell Line CAOV3 Cell Line CAOV3 AR037 cell line PA-1 cell line PA-1 AR038 cell line transformed cell line transformed AR039 colon colon AR040 colon (9808co65R) colon (9808co65R) AR041 colon (9809co15) colon (9809co15) AR042 colon cancer colon cancer AR043 colon cancer (9808co64R) colon cancer (9808co64R) AR044 colon cancer 9809co14 colon cancer 9809co14 AR050 Donor II B Cells 24 hrs Donor II B Cells 24 hrs AR051 Donor II B Cells 72 hrs Donor II B Cells 72 hrs AR052 Donor II B-Cells 24 hrs. Donor II B-Cells 24 hrs. AR053 Donor II B-Cells 72 hrs Donor II B-Cells 72 hrs AR054 Donor II Resting B Cells Donor II Resting B Cells AR055 Heart Heart AR056 Human Lung (clonetech) Human Lung (clonetech) AR057 Human Mammary (CLONTECH ™) Human Mammary (CLONTECH ™) AR058 Human Thymus (clonetech) Human Thymus (clonetech) AR059 Jurkat (unstimulated) Jurkat (unstimulated) AR060 Kidney Kidney AR061 Liver Liver AR062 Liver (CLONTECH ™) Liver (CLONTECH ™) AR063 Lymphocytes chronic lymphocytic Lymphocytes chronic lymphocytic leukaemia leukaemia AR064 Lymphocytes diffuse large B cell Lymphocytes diffuse large B cell lymphoma lymphoma AR065 Lymphocytes follicular lymphoma Lymphocytes follicular lymphoma AR066 normal breast normal breast AR067 Normal Ovarian (4004901) Normal Ovarian (4004901) AR068 Normal Ovary 9508G045 Normal Ovary 9508G045 AR069 Normal Ovary 9701G208 Normal Ovary 9701G208 AR070 Normal Ovary 9806G005 Normal Ovary 9806G005 AR071 Ovarian Cancer Ovarian Cancer AR072 Ovarian Cancer (9702G001) Ovarian Cancer (9702G001) AR073 Ovarian Cancer (9707G029) Ovarian Cancer (9707G029) AR074 Ovarian Cancer (9804G011) Ovarian Cancer (9804G011) AR075 Ovarian Cancer (9806G019) Ovarian Cancer (9806G019) AR076 Ovarian Cancer (9807G017) Ovarian Cancer (9807G017) AR077 Ovarian Cancer (9809G001) Ovarian Cancer (9809G001) AR078 ovarian cancer 15799 ovarian cancer 15799 AR079 Ovarian Cancer 17717AID Ovarian Cancer 17717AID AR080 Ovarian Cancer 4004664B1 Ovarian Cancer 4004664B1 AR081 Ovarian Cancer 4005315A1 Ovarian Cancer 4005315A1 AR082 ovarian cancer 94127303 ovarian cancer 94127303 AR083 Ovarian Cancer 96069304 Ovarian Cancer 96069304 AR084 Ovarian Cancer 9707G029 Ovarian Cancer 9707G029 AR085 Ovarian Cancer 9807G045 Ovarian Cancer 9807G045 AR086 ovarian cancer 9809G001 ovarian cancer 9809G001 AR087 Ovarian Cancer 9905C032RC Ovarian Cancer 9905C032RC AR088 Ovarian cancer 9907 C00 3rd Ovarian cancer 9907 C00 3rd AR089 Prostate Prostate AR090 Prostate (clonetech) Prostate (clonetech) AR091 prostate cancer prostate cancer AR092 prostate cancer #15176 prostate cancer #15176 AR093 prostate cancer #15509 prostate cancer #15509 AR094 prostate cancer #15673 prostate cancer #15673 AR095 Small Intestine (CLONTECH ™) Small Intestine (CLONTECH ™) AR096 Spleen Spleen AR097 Thymus T cells activated Thymus T cells activated AR098 Thymus T cells resting Thymus T cells resting AR099 Tonsil Tonsil AR100 Tonsil geminal center centroblast Tonsil geminal center centroblast AR101 Tonsil germinal center B cell Tonsil germinal center B cell AR102 Tonsil lymph node Tonsil lymph node AR103 Tonsil memory B cell Tonsil memory B cell AR104 Whole Brain Whole Brain AR105 Xenograft ES-2 Xenograft ES-2 AR106 Xenograft SW626 Xenograft SW626 AR119 001: IL-2 001: IL-2 AR120 001: IL-2.1 001: IL-2.1 AR121 001: IL-2_b 001: IL-2_b AR124 002: Monocytes untreated (1 hr) 002: Monocytes untreated (1 hr) AR125 002: Monocytes untreated (5 hrs) 002: Monocytes untreated (5 hrs) AR126 002: Control.1C 002: Control.1C AR127 002: IL2.1C 002: IL2.1C AR130 003: Placebo-treated Rat Lacrimal 003: Placebo-treated Rat Lacrimal Gland Gland AR131 003: Placebo-treated Rat 003: Placebo-treated Rat Submandibular Gland Submandibular Gland AR135 004: Monocytes untreated (5 hrs) 004: Monocytes untreated (5 hrs) AR136 004: Monocytes untreated 1 hr 004: Monocytes untreated 1 hr AR139 005: Placebo (48 hrs) 005: Placebo (48 hrs) AR140 006: pC4 (24 hrs) 006: pC4 (24 hrs) AR141 006: pC4 (48 hrs) 006: pC4 (48 hrs) AR152 007: PHA(1 hr) 007: PHA(1 hr) AR153 007: PHA(6 HRS) 007: PHA(6 HRS) AR154 007: PMA(6 hrs) 007: PMA(6 hrs) AR155 008: 1449_#2 008: 1449_#2 AR161 01: A - max 24 01: A - max 24 AR162 01: A - max 26 01: A - max 26 AR163 01: A - max 30 01: A - max 30 AR164 01: B - max 24 01: B - max 24 AR165 01: B - max 26 01: B - max 26 AR166 01: B - max 30 01: B - max 30 AR167 1449 Sample 1449 Sample AR168 3T3P10 1.0 uM insulin 3T3P10 1.0 uM insulin AR169 3T3P10 10 nM Insulin 3T3P10 10 nM Insulin AR170 3T3P10 10 uM insulin 3T3P10 10 uM insulin AR171 3T3P10 No Insulin 3T3P10 No Insulin AR172 3T3P4 3T3P4 AR173 Adipose (41892) Adipose (41892) AR174 Adipose Diabetic (41611) Adipose Diabetic (41611) AR175 Adipose Diabetic (41661) Adipose Diabetic (41661) AR176 Adipose Diabetic (41689) Adipose Diabetic (41689) AR177 Adipose Diabetic (41706) Adipose Diabetic (41706) AR178 Adipose Diabetic (42352) Adipose Diabetic (42352) AR179 Adipose Diabetic (42366) Adipose Diabetic (42366) AR180 Adipose Diabetic (42452) Adipose Diabetic (42452) AR181 Adipose Diabetic (42491) Adipose Diabetic (42491) AR182 Adipose Normal (41843) Adipose Normal (41843) AR183 Adipose Normal (41893) Adipose Normal (41893) AR184 Adipose Normal (42452) Adipose Normal (42452) AR185 Adrenal Gland Adrenal Gland AR186 Adrenal Gland + Whole Brain Adrenal Gland + Whole Brain AR187 B7(1 hr) + (inverted) B7(1 hr) + (inverted) AR188 Breast (18275A2B) Breast (18275A2B) AR189 Breast (4004199) Breast (4004199) AR190 Breast (4004399) Breast (4004399) AR191 Breast (4004943B7) Breast (4004943B7) AR192 Breast (4005570B1) Breast (4005570B1) AR193 Breast Cancer (4004127A30) Breast Cancer (4004127A30) AR194 Breast Cancer (400443A21) Breast Cancer (400443A21) AR195 Breast Cancer (4004643A2) Breast Cancer (4004643A2) AR196 Breast Cancer (4004710A7) Breast Cancer (4004710A7) AR197 Breast Cancer (4004943A21) Breast Cancer (4004943A21) AR198 Breast Cancer (400553A2) Breast Cancer (400553A2) AR199 Breast Cancer (9805C046R) Breast Cancer (9805C046R) AR200 Breast Cancer (9806C012R) Breast Cancer (9806C012R) AR201 Breast Cancer (ODQ 45913) Breast Cancer (ODQ 45913) AR202 Breast Cancer (ODQ45913) Breast Cancer (ODQ45913) AR203 Breast Cancer (ODQ4591B) Breast Cancer (ODQ4591B) AR204 Colon Cancer (15663) Colon Cancer (15663) AR205 Colon Cancer (4005144A4) Colon Cancer (4005144A4) AR206 Colon Cancer (4005413A4) Colon Cancer (4005413A4) AR207 Colon Cancer (4005570B1) Colon Cancer (4005570B1) AR208 Control RNA #1 Control RNA #1 AR209 Control RNA #2 Control RNA #2 AR210 Cultured Preadipocyte (blue) Cultured Preadipocyte (blue) AR211 Cultured Preadipocyte (Red) Cultured Preadipocyte (Red) AR212 Donor II B-Cells 24 hrs Donor II B-Cells 24 hrs AR213 Donor II Resting B-Cells Donor II Resting B-Cells AR214 H114EP12 10 nM Insulin H114EP12 10 nM Insulin AR215 H114EP12 (10 nM insulin) H114EP12 (10 nM insulin) AR216 H114EP12 (2.6 ug/ul) H114EP12 (2.6 ug/ul) AR217 H114EP12 (3.6 ug/ul) H114EP12 (3.6 ug/ul) AR218 HUVEC #1 HUVEC #1 AR219 HUVEC #2 HUVEC #2 AR221 L6 undiff. L6 undiff. AR222 L6 Undifferentiated L6 Undifferentiated AR223 L6P8 + 10 nM Insulin L6P8 + 10 nM Insulin AR224 L6P8 + HS L6P8 + HS AR225 L6P8 10 nM Insulin L6P8 10 nM Insulin AR226 Liver (00-06-A007B) Liver (00-06-A007B) AR227 Liver (96-02-A075) Liver (96-02-A075) AR228 Liver (96-03-A144) Liver (96-03-A144) AR229 Liver (96-04-A138) Liver (96-04-A138) AR230 Liver (97-10-A074B) Liver (97-10-A074B) AR231 Liver (98-09-A242A) Liver (98-09-A242A) AR232 Liver Diabetic (1042) Liver Diabetic (1042) AR233 Liver Diabetic (41616) Liver Diabetic (41616) AR234 Liver Diabetic (41955) Liver Diabetic (41955) AR235 Liver Diabetic (42352R) Liver Diabetic (42352R) AR236 Liver Diabetic (42366) Liver Diabetic (42366) AR237 Liver Diabetic (42483) Liver Diabetic (42483) AR238 Liver Diabetic (42491) Liver Diabetic (42491) AR239 Liver Diabetic (99-09-A281A) Liver Diabetic (99-09-A281A) AR240 Lung Lung AR241 Lung (27270) Lung (27270) AR242 Lung (2727Q) Lung (2727Q) AR243 Lung Cancer (4005116A1) Lung Cancer (4005116A1) AR244 Lung Cancer (4005121A5) Lung Cancer (4005121A5) AR245 Lung Cancer (4005121A5)) Lung Cancer (4005121A5)) AR246 Lung Cancer (4005340A4) Lung Cancer (4005340A4) AR247 Mammary Gland Mammary Gland AR248 Monocyte (CT) Monocyte (CT) AR249 Monocyte (OCT) Monocyte (OCT) AR250 Monocytes (CT) Monocytes (CT) AR251 Monocytes (INFG 18 hr) Monocytes (INFG 18 hr) AR252 Monocytes (INFG 18 hr) Monocytes (INFG 18 hr) AR253 Monocytes (INFG 8-11) Monocytes (INFG 8-11) AR254 Monocytes (O CT) Monocytes (O CT) AR255 Muscle (91-01-A105) Muscle (91-01-A105) AR256 Muscle (92-04-A059) Muscle (92-04-A059) AR257 Muscle (97-11-A056d) Muscle (97-11-A056d) AR258 Muscle (99-06-A210A) Muscle (99-06-A210A) AR259 Muscle (99-07-A203B) Muscle (99-07-A203B) AR260 Muscle (99-7-A203B) Muscle (99-7-A203B) AR261 Muscle Diabetic (42352R) Muscle Diabetic (42352R) AR262 Muscle Diabetic (42366) Muscle Diabetic (42366) AR263 NK-19 Control NK-19 Control AR264 NK-19 IL Treated 72 hrs NK-19 IL Treated 72 hrs AR265 NK-19 UK Treated 72 hrs. NK-19 UK Treated 72 hrs. AR266 Omentum Normal (94-08-B009) Omentum Normal (94-08-B009) AR267 Omentum Normal (97-01-A039A) Omentum Normal (97-01-A039A) AR268 Omentum Normal (97-04-A114C) Omentum Normal (97-04-A114C) AR269 Omentum Normal (97-06-A117C) Omentum Normal (97-06-A117C) AR270 Omentum Normal (97-09-B004C) Omentum Normal (97-09-B004C) AR271 Ovarian Cancer (17717AID) Ovarian Cancer (17717AID) AR272 Ovarian Cancer (9905C023RC) Ovarian Cancer (9905C023RC) AR273 Ovarian Cancer (9905C032RC) Ovarian Cancer (9905C032RC) AR274 Ovary (9508G045) Ovary (9508G045) AR275 Ovary (9701G208) Ovary (9701G208) AR276 Ovary 9806G005 Ovary 9806G005 AR277 Pancreas Pancreas AR278 Placebo Placebo AR279 rIL2 Control rIL2 Control AR280 RSS288L RSS288L AR281 RSS288LC RSS288LC AR282 Salivary Gland Salivary Gland AR283 Skeletal Muscle Skeletal Muscle AR284 Skeletal Muscle (91-01-A105) Skeletal Muscle (91-01-A105) AR285 Skeletal Muscle (42180) Skeletal Muscle (42180) AR286 Skeletal Muscle (42386) Skeletal Muscle (42386) AR287 Skeletal Muscle (42461) Skeletal Muscle (42461) AR288 Skeletal Muscle (91-01-A105) Skeletal Muscle (91-01-A105) AR289 Skeletal Muscle (92-04-A059) Skeletal Muscle (92-04-A059) AR290 Skeletal Muscle (96-08-A171) Skeletal Muscle (96-08-A171) AR291 Skeletal Muscle (97-07-A190A) Skeletal Muscle (97-07-A190A) AR292 Skeletal Muscle Diabetic (42352) Skeletal Muscle Diabetic (42352) AR293 Skeletal Muscle Diabetic (42366) Skeletal Muscle Diabetic (42366) AR294 Skeletal Muscle Diabetic (42395) Skeletal Muscle Diabetic (42395) AR295 Skeletal Muscle Diabetic (42483) Skeletal Muscle Diabetic (42483) AR296 Skeletal Muscle Diabetic (42491) Skeletal Muscle Diabetic (42491) AR297 Skeletal Muscle Diabetic 42352 Skeletal Muscle Diabetic 42352 AR298 Skeletal Musle (42461) Skeletal Musle (42461) AR299 Small Intestine Small Intestine AR300 Stomach Stomach AR301 T-Cell + HDPBQ71.fc 1449 16 hrs T-Cell + HDPBQ71.fc 1449 16 hrs AR302 T-Cell + HDPBQ71.fc 1449 6 hrs T-Cell + HDPBQ71.fc 1449 6 hrs AR303 T-Cell + IL2 16 hrs T-Cell + IL2 16 hrs AR304 T-Cell + IL2 6 hrs T-Cell + IL2 6 hrs AR306 T-Cell Untreated 16 hrs T-Cell Untreated 16 hrs AR307 T-Cell Untreated 6 hrs T-Cell Untreated 6 hrs AR308 T-Cells 24 hours T-Cells 24 hours AR309 T-Cells 24 hrs T-Cells 24 hrs AR310 T-Cells 24 hrs. T-Cells 24 hrs. AR311 T-Cells 24 hrs T-Cells 24 hrs AR312 T-Cells 4 days T-Cells 4 days AR313 Thymus Thymus AR314 TRE TRE AR315 TREC TREC AR317 B lymphocyte, B lymphocyte, AR318 (non-T; non-B) (non-T; non-B) AR326 001-293 RNA (Vector Control) 001-293 RNA (Vector Control) AR327 001: Control 001: Control AR328 001: Control.1 001: Control.1 AR355 Acute Lymphocyte Leukemia Acute Lymphocyte Leukemia AR356 AML Patient #11 AML Patient #11 AR357 AML Patient #2 AML Patient #2 AR358 AML Patient #2 SGAH AML Patient #2 SGAH AR359 AML Patient#2 AML Patient#2 AR360 Aorta Aorta AR361 B Cell B Cell AR362 B lymphoblast B lymphoblast AR363 B lymphocyte B lymphocyte AR364 B lymphocytes B lymphocytes AR365 B-cell B-cell AR366 B-Cells B-Cells AR367 B-Lymphoblast B-Lymphoblast AR368 B-Lymphocytes B-Lymphocytes AR369 Bladder Bladder AR370 Bone Marrow Bone Marrow AR371 Bronchial Epithelial Cell Bronchial Epithelial Cell AR372 Bronchial Epithelial Cells Bronchial Epithelial Cells AR373 Caco-2A Caco-2A AR374 Caco-2B Caco-2B AR375 Caco-2C Caco-2C AR376 Cardiac #1 Cardiac #1 AR377 Cardiac #2 Cardiac #2 AR378 Chest Muscle Chest Muscle AR381 Dendritic Cell Dendritic Cell AR382 Dendritic cells Dendritic cells AR383 E. coli E. coli AR384 Epithelial Cells Epithelial Cells AR385 Esophagus Esophagus AR386 FPPS FPPS AR387 FPPSC FPPSC AR388 HepG2 Cell Line HepG2 Cell Line AR389 HepG2 Cell line Buffer 1 hr. HepG2 Cell line Buffer 1 hr. AR390 HepG2 Cell line Buffer 06 hr HepG2 Cell line Buffer 06 hr AR391 HepG2 Cell line Buffer 24 hr. HepG2 Cell line Buffer 24 hr. AR392 HepG2 Cell line Insulin 01 hr. HepG2 Cell line Insulin 01 hr. AR393 HepG2 Cell line Insulin 06 hr. HepG2 Cell line Insulin 06 hr. AR394 HepG2 Cell line Insulin 24 hr. HepG2 Cell line Insulin 24 hr. AR398 HMC-1 HMC-1 AR399 HMCS HMCS AR400 HMSC HMSC AR401 HUVEC #3 HUVEC #3 AR402 HUVEC #4 HUVEC #4 AR404 KIDNEY NORMAL KIDNEY NORMAL AR405 KIDNEY TUMOR KIDNEY TUMOR AR406 KIDNEY TUMOR AR407 Lymph Node Lymph Node AR408 Macrophage Macrophage AR409 Megakarioblast Megakarioblast AR410 Monocyte Monocyte AR411 Monocytes Monocytes AR412 Myocardium Myocardium AR413 Myocardium #3 Myocardium #3 AR414 Myocardium #4 Myocardium #4 AR415 Myocardium #5 Myocardium #5 AR416 NK NK AR417 NK cell NK cell AR418 NK cells NK cells AR419 NKYa NKYa AR420 NKYa019 NKYa019 AR421 Ovary Ovary AR422 Patient #11 Patient #11 AR423 Peripheral blood Peripheral blood AR424 Primary Adipocytes Primary Adipocytes AR425 Promyeloblast Promyeloblast AR427 RSSWT RSSWT AR428 RSSWTC RSSWTC AR429 SW 480(G1) SW 480(G1) AR430 SW 480(G2) SW 480(G2) AR431 SW 480(G3) SW 480(G3) AR432 SW 480(G4) SW 480(G4) AR433 SW 480(G5) SW 480(G5) AR434 T Lymphoblast T Lymphoblast AR435 T Lymphocyte T Lymphocyte AR436 T-Cell T-Cell AR438 T-Cell, T-Cell, AR439 T-Cells T-Cells AR440 T-lymphoblast T-lymphoblast AR441 Th 1 Th 1 AR442 Th 2 Th 2 AR443 Th1 Th1 AR444 Th2 Th2 H0002 Human Adult Heart Human Adult Heart Heart Uni-ZAP XR H0004 Human Adult Spleen Human Adult Spleen Spleen Uni-ZAP XR H0007 Human Cerebellum Human Cerebellum Brain Uni-ZAP XR H0008 Whole 6 Week Old Embryo Uni-ZAP XR H0009 Human Fetal Brain Uni-ZAP XR H0011 Human Fetal Kidney Human Fetal Kidney Kidney Uni-ZAP XR H0012 Human Fetal Kidney Human Fetal Kidney Kidney Uni-ZAP XR H0013 Human 8 Week Whole Embryo Human 8 Week Old Embryo Embryo Uni-ZAP XR H0014 Human Gall Bladder Human Gall Bladder Gall Bladder Uni-ZAP XR H0015 Human Gall Bladder, fraction II Human Gall Bladder Gall Bladder Uni-ZAP XR H0016 Human Greater Omentum Human Greater Omentum peritoneum Uni-ZAP XR H0017 Human Greater Omentum Human Greater Omentum peritoneum Uni-ZAP XR H0020 Human Hippocampus Human Hippocampus Brain Uni-ZAP XR H0022 Jurkat Cells Jurkat T-Cell Line Lambda ZAP II H0023 Human Fetal Lung Uni-ZAP XR H0024 Human Fetal Lung III Human Fetal Lung Lung Uni-ZAP XR H0025 Human Adult Lymph Node Human Adult Lymph Node Lymph Node Lambda ZAP II H0026 Namalwa Cells Namalwa B-Cell Line, EBV Lambda ZAP II immortalized H0030 Human Placenta Uni-ZAP XR H0031 Human Placenta Human Placenta Placenta Uni-ZAP XR H0032 Human Prostate Human Prostate Prostate Uni-ZAP XR H0033 Human Pituitary Human Pituitary Uni-ZAP XR H0036 Human Adult Small Intestine Human Adult Small Intestine Small Int. Uni-ZAP XR H0038 Human Testes Human Testes Testis Uni-ZAP XR H0039 Human Pancreas Tumor Human Pancreas Tumor Pancreas disease Uni-ZAP XR H0040 Human Testes Tumor Human Testes Tumor Testis disease Uni-ZAP XR H0041 Human Fetal Bone Human Fetal Bone Bone Uni-ZAP XR H0042 Human Adult Pulmonary Human Adult Pulmonary Lung Uni-ZAP XR H0044 Human Cornea Human Cornea eye Uni-ZAP XR H0045 Human Esophagus, Cancer Human Esophagus, cancer Esophagus disease Uni-ZAP XR H0046 Human Endometrial Tumor Human Endometrial Tumor Uterus disease Uni-ZAP XR H0047 Human Fetal Liver Human Fetal Liver Liver Uni-ZAP XR H0048 Human Pineal Gland Human Pineal Gland Uni-ZAP XR H0050 Human Fetal Heart Human Fetal Heart Heart Uni-ZAP XR H0051 Human Hippocampus Human Hippocampus Brain Uni-ZAP XR H0052 Human Cerebellum Human Cerebellum Brain Uni-ZAP XR H0056 Human Umbilical Vein, Endo. Human Umbilical Vein Endothelial Umbilical Uni-ZAP XR remake Cells vein H0057 Human Fetal Spleen Uni-ZAP XR H0058 Human Thymus Tumor Human Thymus Tumor Thymus disease Lambda ZAP II H0059 Human Uterine Cancer Human Uterine Cancer Uterus disease Lambda ZAP II H0060 Human Macrophage Human Macrophage Blood Cell Line pBLUESCRIPT ™ H0061 Human Macrophage Human Macrophage Blood Cell Line pBLUESCRIPT ™ H0063 Human Thymus Human Thymus Thymus Uni-ZAP XR H0065 Human Esophagus, Normal Human Esophagus, normal Esophagus Uni-ZAP XR H0068 Human Skin Tumor Human Skin Tumor Skin disease Uni-ZAP XR H0069 Human Activated T-Cells Activated T-Cells Blood Cell Line Uni-ZAP XR H0070 Human Pancreas Human Pancreas Pancreas Uni-ZAP XR H0071 Human Infant Adrenal Gland Human Infant Adrenal Gland Adrenal Uni-ZAP XR gland H0075 Human Activated T-Cells (II) Activated T-Cells Blood Cell Line Uni-ZAP XR H0076 Human Membrane Bound Human Membrane Bound Blood Cell Line Uni-ZAP XR Polysomes Polysomes H0078 Human Lung Cancer Human Lung Cancer Lung disease Lambda ZAP II H0081 Human Fetal Epithelium (Skin) Human Fetal Skin Skin Uni-ZAP XR H0083 Human JURKAT MEMBRANE Jurkat Cells Uni-ZAP XR BOUND POLYSOMES H0085 Human Colon Human Colon Lambda ZAP II H0086 Human epithelioid sarcoma Epithelioid Sarcoma, muscle Sk Muscle disease Uni-ZAP XR H0087 Human Thymus Human Thymus pBLUESCRIPT ™ H0090 Human T-Cell Lymphoma T-Cell Lymphoma T-Cell disease Uni-ZAP XR H0097 Human Adult Heart, subtracted Human Adult Heart Heart pBLUESCRIPT ™ H0098 Human Adult Liver, subtracted Human Adult Liver Liver Uni-ZAP XR H0099 Human Lung Cancer, subtracted Human Lung Cancer Lung pBLUESCRIPT ™ H0100 Human Whole Six Week Old Human Whole Six Week Old Embryo Uni-ZAP XR Embryo Embryo H0102 Human Whole 6 Week Old Embryo Human Whole Six Week Old Embryo pBLUESCRIPT ™ (II), subt Embryo H0103 Human Fetal Brain, subtracted Human Fetal Brain Brain Uni-ZAP XR H0107 Human Infant Adrenal Gland, Human Infant Adrenal Gland Adrenal pBLUESCRIPT ™ subtracted gland H0108 Human Adult Lymph Node, Human Adult Lymph Node Lymph Node Uni-ZAP XR subtracted H0109 Human Macrophage, subtracted Macrophage Blood Cell Line pBLUESCRIPT ™ H0110 Human Old Ovary, subtracted Human Old Ovary Ovary pBLUESCRIPT ™ H0111 Human Placenta, subtracted Human Placenta Placenta pBLUESCRIPT ™ H0116 Human Thymus Tumor, subtracted Human Thymus Tumor Thymus pBLUESCRIPT ™ H0118 Human Adult Kidney Human Adult Kidney Kidney Uni-ZAP XR H0120 Human Adult Spleen, subtracted Human Adult Spleen Spleen Uni-ZAP XR H0121 Human Cornea, subtracted Human Cornea eye Uni-ZAP XR H0122 Human Adult Skeletal Muscle Human Skeletal Muscle Sk Muscle Uni-ZAP XR H0123 Human Fetal Dura Mater Human Fetal Dura Mater Brain Uni-ZAP XR H0124 Human Rhabdomyosarcoma Human Rhabdomyosarcoma Sk Muscle disease Uni-ZAP XR H0125 Cem cells cyclohexamide treated Cyclohexamide Treated Cem, Blood Cell Line Uni-ZAP XR Jurkat, Raji, and Supt H0128 Jurkat cells, thiouridine activated Jurkat Cells Uni-ZAP XR H0130 LNCAP untreated LNCAP Cell Line Prostate Cell Line Uni-ZAP XR H0131 LNCAP + o.3 nM R1881 LNCAP Cell Line Prostate Cell Line Uni-ZAP XR H0132 LNCAP + 30 nM R1881 LNCAP Cell Line Prostate Cell Line Uni-ZAP XR H0134 Raji Cells, cyclohexamide treated Cyclohexamide Treated Cem, Blood Cell Line Uni-ZAP XR Jurkat, Raji, and Supt H0135 Human Synovial Sarcoma Human Synovial Sarcoma Synovium Uni-ZAP XR H0136 Supt Cells, cyclohexamide treated Cyclohexamide Treated Cem, Blood Cell Line Uni-ZAP XR Jurkat, Raji, and Supt H0139 Activated T-Cells, 4 hrs. Activated T-Cells Blood Cell Line Uni-ZAP XR H0140 Activated T-Cells, 8 hrs. Activated T-Cells Blood Cell Line Uni-ZAP XR H0141 Activated T-Cells, 12 hrs. Activated T-Cells Blood Cell Line Uni-ZAP XR H0144 Nine Week Old Early Stage Human 9 Wk Old Early Stage Human Embryo Uni-ZAP XR H0147 Human Adult Liver Human Adult Liver Liver Uni-ZAP XR H0149 7 Week Old Early Stage Human, Human Whole 7 Week Old Embryo Uni-ZAP XR subtracted Embryo H0150 Human Epididymus Epididymis Testis Uni-ZAP XR H0151 Early Stage Human Liver Human Fetal Liver Liver Uni-ZAP XR H0154 Human Fibrosarcoma Human Skin Fibrosarcoma Skin disease Uni-ZAP XR H0156 Human Adrenal Gland Tumor Human Adrenal Gland Tumor Adrenal disease Uni-ZAP XR Gland H0158 Activated T-Cells, 4 hrs., ligation 2 Activated T-Cells Blood Cell Line Uni-ZAP XR H0159 Activated T-Cells, 8 hrs., ligation 2 Activated T-Cells Blood Cell Line Uni-ZAP XR H0161 Activated T-Cells, 24 hrs., ligation 2 Activated T-Cells Blood Cell Line Uni-ZAP XR H0163 Human Synovium Human Synovium Synovium Uni-ZAP XR H0165 Human Prostate Cancer, Stage B2 Human Prostate Cancer, stage B2 Prostate disease Uni-ZAP XR H0166 Human Prostate Cancer, Stage B2 Human Prostate Cancer, stage B2 Prostate disease Uni-ZAP XR fraction H0167 Activated T-Cells, 24 hrs. Activated T-Cells Blood Cell Line Uni-ZAP XR H0169 Human Prostate Cancer, Stage C Human Prostate Cancer, stage C Prostate disease Uni-ZAP XR fraction H0170 12 Week Old Early Stage Human Twelve Week Old Early Stage Embryo Uni-ZAP XR Human H0171 12 Week Old Early Stage Human, II Twelve Week Old Early Stage Embryo Uni-ZAP XR Human H0172 Human Fetal Brain, random primed Human Fetal Brain Brain Lambda ZAP II H0176 CAMA1Ee Cell Line CAMA1Ee Cell Line Breast Cell Line Uni-ZAP XR H0177 CAMA1Ee Cell Line CAMA1Ee Cell Line Breast Cell Line Uni-ZAP XR H0178 Human Fetal Brain Human Fetal Brain Brain Uni-ZAP XR H0179 Human Neutrophil Human Neutrophil Blood Cell Line Uni-ZAP XR H0180 Human Primary Breast Cancer Human Primary Breast Cancer Breast disease Uni-ZAP XR H0181 Human Primary Breast Cancer Human Primary Breast Cancer Breast disease Uni-ZAP XR H0182 Human Primary Breast Cancer Human Primary Breast Cancer Breast disease Uni-ZAP XR H0183 Human Colon Cancer Human Colon Cancer Colon disease Uni-ZAP XR H0184 Human Colon Cancer, metasticized Human Colon Cancer, metasticized Liver disease Lambda ZAP II to live to liver H0187 Resting T-Cell T-Cells Blood Cell Line Lambda ZAP II H0188 Human Normal Breast Human Normal Breast Breast Uni-ZAP XR H0189 Human Resting Macrophage Human Macrophage/Monocytes Blood Cell Line Uni-ZAP XR H0190 Human Activated Macrophage Human Macrophage/Monocytes Blood Cell Line Uni-ZAP XR (LPS) H0192 Cem Cells, cyclohexamide treated, Cyclohexamide Treated Cem, Blood Cell Line Uni-ZAP XR subtra Jurkat, Raji, and Supt H0194 Human Cerebellum, subtracted Human Cerebellum Brain pBLUESCRIPT ™ H0196 Human Cardiomyopathy, subtracted Human Cardiomyopathy Heart Uni-ZAP XR H0197 Human Fetal Liver, subtracted Human Fetal Liver Liver Uni-ZAP XR H0199 Human Fetal Liver, subtracted, neg Human Fetal Liver Liver Uni-ZAP XR clone H0200 Human Greater Omentum, fract II Human Greater Omentum peritoneum Uni-ZAP XR remake, H0201 Human Hippocampus, subtracted Human Hippocampus Brain pBLUESCRIPT ™ H0202 Jurkat Cells, cyclohexamide treated, Cyclohexamide Treated Cem, Blood Cell Line Uni-ZAP XR subtraction Jurkat, Raji, and Supt H0204 Human Colon Cancer, subtracted Human Colon Cancer Colon pBLUESCRIPT ™ H0205 Human Colon Cancer, differential Human Colon Cancer Colon pBLUESCRIPT ™ H0207 LNCAP, differential expression LNCAP Cell Line Prostate Cell Line pBLUESCRIPT ™ H0208 Early Stage Human Lung, subtracted Human Fetal Lung Lung pBLUESCRIPT ™ H0209 Human Cerebellum, differentially Human Cerebellum Brain Uni-ZAP XR expressed H0211 Human Prostate, differential Human Prostate Prostate pBLUESCRIPT ™ expression H0212 Human Prostate, subtracted Human Prostate Prostate pBLUESCRIPT ™ H0213 Human Pituitary, subtracted Human Pituitary Uni-ZAP XR H0214 Raji cells, cyclohexamide treated, Cyclohexamide Treated Cem, Blood Cell Line pBLUESCRIPT ™ subtracted Jurkat, Raji, and Supt H0215 Raji cells, cyclohexamide treated, Cyclohexamide Treated Cem, Blood Cell Line pBLUESCRIPT ™ differentially expressed Jurkat, Raji, and Supt H0216 Supt cells, cyclohexamide treated, Cyclohexamide Treated Cem, Blood Cell Line pBLUESCRIPT ™ subtracted Jurkat, Raji, and Supt H0217 Supt cells, cyclohexamide treated, Cyclohexamide Treated Cem, Blood Cell Line pBLUESCRIPT ™ differentially expressed Jurkat, Raji, and Supt H0218 Activated T-Cells, 0 hrs, subtracted Activated T-Cells Blood Cell Line Uni-ZAP XR H0219 Activated T-Cells, 0 hrs, Activated T-Cells Blood Cell Line Uni-ZAP XR differentially expressed H0220 Activated T-Cells, 4 hrs, subtracted Activated T-Cells Blood Cell Line Uni-ZAP XR H0222 Activated T-Cells, 8 hrs, subtracted Activated T-Cells Blood Cell Line Uni-ZAP XR H0223 Activated T-Cells, 8 hrs, Activated T-Cells Blood Cell Line Uni-ZAP XR differentially expressed H0224 Activated T-Cells, 12 hrs, subtracted Activated T-Cells Blood Cell Line Uni-ZAP XR H0225 Activated T-Cells, 12 hrs, Activated T-Cells Blood Cell Line Uni-ZAP XR differentially expressed H0229 Early Stage Human Brain, random Early Stage Human Brain Brain Lambda ZAP II primed H0230 Human Cardiomyopathy, diff exp Human Cardiomyopathy Heart disease Uni-ZAP XR H0231 Human Colon, subtraction Human Colon pBLUESCRIPT ™ H0232 Human Colon, differential Human Colon pBLUESCRIPT ™ expression H0234 human colon cancer, metastatic to Human Colon Cancer, metasticized Liver pBLUESCRIPT ™ liver, differentially expressed to liver H0235 Human colon cancer, metaticized to Human Colon Cancer, metasticized Liver pBLUESCRIPT ™ liver, subtraction to liver H0239 Human Kidney Tumor Human Kidney Tumor Kidney disease Uni-ZAP XR H0240 C7MCF7 cell line, estrogen treated, C7MCF7 Cell Line, estrogen Breast Cell Line Uni-ZAP XR Differential treated H0241 C7MCF7 cell line, estrogen treated, C7MCF7 Cell Line, estrogen Breast Cell Line Uni-ZAP XR subtraction treated H0242 Human Fetal Heart, Differential Human Fetal Heart Heart pBLUESCRIPT ™ (Fetal-Specific) H0244 Human 8 Week Whole Embryo, Human 8 Week Old Embryo Embryo Uni-ZAP XR subtracted H0246 Human Fetal Liver- Enzyme Human Fetal Liver Liver Uni-ZAP XR subtraction H0247 Human Membrane Bound Human Membrane Bound Blood Cell Line Uni-ZAP XR Polysomes- Enzyme Subtraction Polysomes H0249 HE7, subtracted by hybridization Human Whole 7 Week Old Embryo Uni-ZAP XR with E7 cDNA Embryo H0250 Human Activated Monocytes Human Monocytes Uni-ZAP XR H0251 Human Chondrosarcoma Human Chondrosarcoma Cartilage disease Uni-ZAP XR H0252 Human Osteosarcoma Human Osteosarcoma Bone disease Uni-ZAP XR H0253 Human adult testis, large inserts Human Adult Testis Testis Uni-ZAP XR H0254 Breast Lymph node cDNA library Breast Lymph Node Lymph Node Uni-ZAP XR H0255 breast lymph node CDNA library Breast Lymph Node Lymph Node Lambda ZAP II H0256 HL-60, unstimulated Human HL-60 Cells, unstimulated Blood Cell Line Uni-ZAP XR H0257 HL-60, PMA 4H HL-60 Cells, PMA stimulated 4H Blood Cell Line Uni-ZAP XR H0261 H. cerebellum, Enzyme subtracted Human Cerebellum Brain Uni-ZAP XR H0263 human colon cancer Human Colon Cancer Colon disease Lambda ZAP II H0264 human tonsils Human Tonsil Tonsil Uni-ZAP XR H0265 Activated T-Cell (12 hs)/Thiouridine T-Cells Blood Cell Line Uni-ZAP XR labelledEco H0266 Human Microvascular Endothelial HMEC Vein Cell Line Lambda ZAP II Cells, fract. A H0267 Human Microvascular Endothelial HMEC Vein Cell Line Lambda ZAP II Cells, fract. B H0268 Human Umbilical Vein Endothelial HUVE Cells Umbilical Cell Line Lambda ZAP II Cells, fract. A vein H0269 Human Umbilical Vein Endothelial HUVE Cells Umbilical Cell Line Lambda ZAP II Cells, fract. B vein H0270 HPAS (human pancreas, subtracted) Human Pancreas Pancreas Uni-ZAP XR H0271 Human Neutrophil, Activated Human Neutrophil - Activated Blood Cell Line Uni-ZAP XR H0272 HUMAN TONSILS, FRACTION 2 Human Tonsil Tonsil Uni-ZAP XR H0274 Human Adult Spleen, fractionII Human Adult Spleen Spleen Uni-ZAP XR H0275 Human Infant Adrenal Gland, Human Infant Adrenal Gland Adrenal pBLUESCRIPT ™ Subtracted gland H0280 K562 + PMA (36 hrs) K562 Cell line cell line Cell Line ZAP Express H0281 Lymph node, abnorm. cell line Lymph Node, abnormal cell line Lymph Node Cell Line ZAP Express (ATCC ™ #7225) H0282 HBGB''s differential consolidation Human Primary Breast Cancer Breast Uni-ZAP XR H0284 Human OB MG63 control fraction I Human Osteoblastoma MG63 cell Bone Cell Line Uni-ZAP XR line H0286 Human OB MG63 treated (10 nM Human Osteoblastoma MG63 cell Bone Cell Line Uni-ZAP XR E2) fraction I line H0288 Human OB HOS control fraction I Human Osteoblastoma HOS cell Bone Cell Line Uni-ZAP XR line H0290 Human OB HOS treated (1 nM E2) Human Osteoblastoma HOS cell Bone Cell Line Uni-ZAP XR fraction I line H0292 Human OB HOS treated (10 nM E2) Human Gsteoblastoma HOS cell Bone Cell Line Uni-ZAP XR fraction I line H0293 WI 38 cells Uni-ZAP XR H0294 Amniotic Cells - TNF induced Amniotic Cells - TNF induced Placenta Cell Line Uni-ZAP XR H0295 Amniotic Cells - Primary Culture Amniotic Cells - Primary Culture Placenta Cell Line Uni-ZAP XR H0300 CD34 positive cells (Cord Blood) CD34 Positive Cells Cord Blood ZAP Express H0305 CD34 positive cells (Cord Blood) CD34 Positive Cells Cord Blood ZAP Express H0306 CD34 depleted Buffy Coat (Cord CD34 Depleted Buffy Coat (Cord Cord Blood ZAP Express Blood) Blood) H0309 Human Chronic Synovitis Synovium, Chronic Synovitis/ Synovium disease Uni-ZAP XR Osteoarthritis H0310 human caudate nucleus Brain Brain Uni-ZAP XR H0316 HUMAN STOMACH Human Stomach Stomach Uni-ZAP XR H0318 HUMAN B CELL LYMPHOMA Human B Cell Lymphoma Lymph Node disease Uni-ZAP XR H0320 Human frontal cortex Human Frontal Cortex Brain Uni-ZAP XR H0321 HUMAN SCHWANOMA Schwanoma Nerve disease Uni-ZAP XR H0327 human copus colosum Human Copus Callosum Brain Uni-ZAP XR H0328 human ovarian cancer Ovarian Cancer Ovary disease Uni-ZAP XR H0329 Dermatofibrosarcoma Protuberance Dermatofibrosarcoma Protuberans Skin disease Uni-ZAP XR H0331 Hepatocellular Tumor Hepatocellular Tumor Liver disease Lambda ZAP II H0333 Hemangiopericytoma Hemangiopericytoma Blood vessel disease Lambda ZAP II H0334 Kidney cancer Kidney Cancer Kidney disease Uni-ZAP XR H0339 Duodenum Duodenum Uni-ZAP XR H0341 Bone Marrow Cell Line (RS4; 11) Bone Marrow Cell Line RS4; 11 Bone Cell Line Uni-ZAP XR Marrow H0342 Lingual Gyrus Lingual Gyrus Brain Uni-Zap XR H0343 stomach cancer (human) Stomach Cancer - 5383A (human) disease Uni-ZAP XR H0344 Adipose tissue (human) Adipose - 6825A (human) Uni-ZAP XR H0345 SKIN Skin - 4000868H Skin Uni-ZAP XR H0346 Brain-medulloblastoma Brain (Medulloblastoma)- Brain disease Uni-ZAP XR 9405C006R H0349 human adult liver cDNA library Human Adult Liver Liver pCMVSport 1 H0350 Human Fetal Liver, mixed 10 & 14 Human Fetal Liver, mixed 10&14 Liver Uni-ZAP XR week Week H0351 Glioblastoma Glioblastoma Brain disease Uni-ZAP XR H0352 wilm''s tumor Wilm''s Tumor disease Uni-ZAP XR H0354 Human Leukocytes Human Leukocytes Blood Cell Line pCMVSport 1 H0355 Human Liver Human Liver, normal Adult pCMVSport 1 H0356 Human Kidney Human Kidney Kidney pCMVSport 1 H0357 H. Normalized Fetal Liver, II Human Fetal Liver Liver Uni-ZAP XR H0359 KMH2 cell line KMH2 ZAP Express H0360 Hemangiopericytoma Hemangiopericytoma disease H0361 Human rejected kidney Human Rejected Kidney disease pBLUESCRIPT ™ H0362 HeLa cell line HELA CELL LINE pSport1 H0366 L428 cell line L428 ZAP Express H0369 H. Atrophic Endometrium Atrophic Endometrium and Uni-ZAP XR myometrium H0370 H. Lymph node breast Cancer Lymph node with Met. Breast disease Uni-ZAP XR Cancer H0372 Human Testes Human Testes Testis pCMVSport 1 H0373 Human Heart Human Adult Heart Heart pCMVSport 1 H0374 Human Brain Human Brain pCMVSport 1 H0375 Human Lung Human Lung pCMVSport 1 H0376 Human Spleen Human Adult Spleen Spleen pCMVSport 1 H0379 Human Tongue, frac 1 Human Tongue pSport1 H0380 Human Tongue, frac 2 Human Tongue pSport1 H0381 Bone Cancer Bone Cancer disease Uni-ZAP XR H0383 Human Prostate BPH, re-excision Human Prostate BPH Uni-ZAP XR H0384 Brain, Kozak Human Brain pCMVSport 1 H0386 Leukocyte and Lung; 4 screens Human Leukocytes Blood Cell Line pCMVSport 1 H0388 Human Rejected Kidney, 704 re- Human Rejected Kidney disease pBLUESCRIPT ™ excision H0390 Human Amygdala Depression, re- Human Amygdala Depression disease pBLUESCRIPT ™ excision H0391 H. Meniingima, M6 Human Meningima brain pSport1 H0392 H. Meningima, M1 Human Meningima brain pSport1 H0393 Fetal Liver, subtraction II Human Fetal Liver Liver pBLUESCRIPT ™ H0394 A-14 cell line Redd-Sternberg cell ZAP Express H0395 A1-CELL LINE Redd-Sternberg cell ZAP Express H0396 L1 Cell line Redd-Sternberg cell ZAP Express H0399 Human Kidney Cortex, re-rescue Human Kidney Cortex Lambda ZAP II H0400 Human Striatum Depression, re- Human Brain, Striatum Depression Brain Lambda ZAP II rescue H0402 CD34 depleted Buffy Coat (Cord CD34 Depleted Buffy Coat (Cord Cord Blood ZAP Express Blood), re-excision Blood) H0403 H. Umbilical Vein Endothelial HUVE Cells Umbilical Cell Line Uni-ZAP XR Cells, IL4 induced vein H0404 H. Umbilical Vein endothelial cells, HUVE Cells Umbilical Cell Line Uni-ZAP XR uninduced vein H0405 Human Pituitary, subtracted VI Human Pituitary pBLUESCRIPT ™ H0406 H Amygdala Depression, subtracted Human Amygdala Depression Uni-ZAP XR H0408 Human kidney Cortex, subtracted Human Kidney Cortex pBLUESCRIPT ™ H0409 H. Striatum Depression, subtracted Human Brain, Striatum Depression Brain pBLUESCRIPT ™ H0410 H. Male bladder, adult H Male Bladder, Adult Bladder pSport1 H0411 H Female Bladder, Adult Human Female Adult Bladder Bladder pSport1 H0412 Human umbilical vein endothelial HUVE Cells Umbilical Cell Line pSport1 cells, IL-4 induced vein H0413 Human Umbilical Vein Endothelial HUVE Cells Umbilical Cell Line pSport1 Cells, uninduced vein H0414 Ovarian Tumor I, OV5232 Ovarian Tumor, OV5232 Ovary disease pSport1 H0415 H. Ovarian Tumor, II, OV5232 Ovarian Tumor, OV5232 Ovary disease pCMVSport 2.0 H0416 Human Neutrophils, Activated, re- Human Neutrophil - Activated Blood Cell Line pBLUESCRIPT ™ excision H0417 Human Pituitary, subtracted VIII Human Pituitary pBLUESCRIPT ™ H0418 Human Pituitary, subtracted VII Human Pituitary PBLUESCRIPT ™ H0419 Bone Cancer, re-excision Bone Cancer Uni-ZAP XR H0421 Human Bone Marrow, re-excision Bone Marrow pBLUESCRIPT ™ H0422 T-Cell PHA 16 hrs T-Cells Blood Cell Line pSport1 H0423 T-Cell PHA 24 hrs T-Cells Blood Cell Line pSport1 H0424 Human Pituitary, subt IX Human Pituitary pBLUESCRIPT ™ H0427 Human Adipose Human Adipose, left hiplipoma pSport1 H0428 Human Ovary Human Ovary Tumor Ovary pSport1 H0429 K562 + PMA (36 hrs), re-excision K562 Cell line cell line Cell Line ZAP Express H0431 H. Kidney Medulla, re-excision Kidney medulla Kidney pBLUESCRIPT ™ H0433 Human Umbilical Vein Endothelial HUVE Cells Umbilical Cell Line pBLUESCRIPT ™ cells, frac B, re-excision vein H0434 Human Brain, striatum, re-excision Human Brain, Striatum pBLUESCRIPT ™ H0435 Ovarian Tumor 10-3-95 Ovarian Tumor, OV350721 Ovary pCMVSport 2.0 H0436 Resting T-Cell Library, II T-Cells Blood Cell Line pSport1 H0437 H Umbilical Vein Endothelial Cells, HUVE Cells Umbilical Cell Line Lambda ZAP II frac A, re-excision vein H0438 H. Whole Brain #2, re-excision Human Whole Brain #2 ZAP Express H0439 Human Eosinophils Eosinophils pBLUESCRIPT ™ H0441 H. Kidney Cortex, subtracted Kidney cortex Kidney pBLUESCRIPT ™ H0443 H. Adipose, subtracted Human Adipose, left hiplipoma pSport1 H0444 Spleen metastic melanoma Spleen, Metastic malignant Spleen disease pSport1 melanoma H0445 Spleen, Chronic lymphocytic Human Spleen, CLL Spleen disease pSport1 leukemia H0449 CD34+ cell, I CD34 positive cells pSport1 H0455 H. Striatum Depression, subt Human Brain, Striatum Depression Brain pBLUESCRIPT ™ H0457 Human Eosinophils Human Eosinophils pSport1 H0458 CD34+ cell, I, frac II CD34 positive cells pSport1 H0459 CD34+cells, II, FRACTION 2 CD34 positive cells pCMVSport 2.0 H0461 H. Kidney Medulla, subtracted Kidney medulla Kidney pBLUESCRIPT ™ H0462 H. Amygdala Depression, subtracted Brain pBLUESCRIPT ™ H0477 Human Tonsil, Lib 3 Human Tonsil Tonsil pSport1 H0478 Salivary Gland, Lib 2 Human Salivary Gland Salivary pSport1 gland H0479 Salivary Gland, Lib 3 Human Salivary Gland Salivary pSport1 gland H0483 Breast Cancer cell line, MDA 36 Breast Cancer Cell line, MDA 36 pSport1 H0484 Breast Cancer Cell line, angiogenic Breast Cancer Cell line, pSport1 Angiogenic, 36T3 H0485 Hodgkin''s Lymphoma I Hodgkin''s Lymphoma I disease pCMVSport 2.0 H0486 Hodgkin''s Lymphoma II Hodgkin''s Lymphoma II disease pCMVSport 2.0 H0487 Human Tonsils, lib I Human Tonsils pCMVSport 2.0 H0488 Human Tonsils, Lib 2 Human Tonsils pCMVSport 2.0 H0489 Crohn''s Disease Ileum Intestine disease pSport1 H0490 Hl-60, untreated, subtracted Human HL-60 Cells, unstimulated Blood Cell Line Uni-ZAP XR H0491 HL-60, PMA 4 H, subtracted HL-60 Cells, PMA stimulated 4 H Blood Cell Line Uni-ZAP XR H0492 HL-60, RA 4 h, Subtracted HL-60 Cells, RA stimulated Blood Cell Line Uni-ZAP XR for 4 H H0494 Keratinocyte Keratinocyte pCMVSport 2.0 H0497 HEL cell line HEL cell line HEL pSport1 92.1.7 H0505 Human Astrocyte Human Astrocyte pSport1 H0506 Ulcerative Colitis Colon Colon pSport1 H0509 Liver, Hepatoma Human Liver, Hepatoma, patient 8 Liver disease pCMVSport 3.0 H0510 Human Liver, normal Human Liver, normal, Patient # 8 Liver pCMVSport 3.0 H0512 Keratinocyte, lib 3 Keratinocyte pCMVSport 2.0 H0518 pBMC stimulated w/ poly I/C pBMC stimulated with poly I/C pCMVSport 3.0 H0519 NTERA2, control NTERA2, Teratocarcinoma pCMVSport 3.0 cell line H0520 NTERA2 + retinoic acid, 14 days NTERA2, Teratocarcinoma pSport1 cell line H0521 Primary Dendritic Cells, lib 1 Primary Dendritic cells pCMVSport 3.0 H0522 Primary Dendritic cells, frac 2 Primary Dendritic cells pCMVSport 3.0 H0525 PCR, pBMC I/C treated pBMC stimulated with poly I/C PCRII H0528 Poly[I]/Poly[C] Normal Lung Poly[I]/Poly[C] Normal Lung pCMVSport 3.0 Fibroblasts Fibroblasts H0529 Myoloid Progenitor Cell Line TF-1 Cell Line; Myoloid pCMVSport 3.0 progenitor cell line H0530 Human Dermal Endothelial Human Dermal Endothelial Cells; pSport1 Cells, untreated untreated H0538 Merkel Cells Merkel cells Lymph node pSport1 H0539 Pancreas Islet Cell Tumor Pancreas Islet Cell Tumour Pancreas disease pSport1 H0540 Skin, burned Skin, leg burned Skin pSport1 H0542 T Cell helper I Helper T cell pCMVSport 3.0 H0543 T cell helper II Helper T cell pCMVSport 3.0 H0544 Human endometrial stromal cells Human endometrial stromal cells pCMVSport 3.0 H0545 Human endometrial stromal cells- Human endometrial stromal cells- pCMVSport 3.0 treated with progesterone treated with proge H0546 Human endometrial stromal cells- Human endometrial stromal cells- pCMVSport 3.0 treated with estradiol treated with estra H0547 NTERA2 teratocarcinoma cell NTERA2, Teratocarcinoma pSport1 line + retinoic acid (14 days) cell line H0549 H. Epididiymus, caput & corpus Human Epididiymus, caput and Uni-ZAP XR corpus H0550 H. Epididiymus, cauda Human Epididiymus, cauda Uni-ZAP XR H0551 Human Thymus Stromal Cells Human Thymus Stromal Cells pCMVSport 3.0 H0553 Human Placenta Human Placenta pCMVSport 3.0 H0555 Rejected Kidney, lib 4 Human Rejected Kidney Kidney disease pCMVSport 3.0 H0556 Activated T-cell(12 h)/Thiouridine- T-Cells Blood Cell Line Uni-ZAP XR re-excision H0559 HL-60, PMA 4 H, re-excision HL-60 Cells, PMA stimulated 4 H Blood Cell Line Uni-ZAP XR H0560 KMH2 KMH2 pCMVSport 3.0 H0561 L428 L428 pCMVSport 3.0 H0562 Human Fetal Brain, normalized c5- Human Fetal Brain pCMVSport 2.0 11-26 H0563 Human Fetal Brain, normalized Human Fetal Brain pCMVSport 2.0 50021F H0564 Human Fetal Brain, normalized Human Fetal Brain pCMVSport 2.0 C5001F H0566 Human Fetal Brain, normalized c50F Human Fetal Brain pCMVSport 2.0 H0567 Human Fetal Brain, normalized Human Fetal Brain pCMVSport 2.0 A5002F H0569 Human Fetal Brain, normalized CO Human Fetal Brain pCMVSport 2.0 H0570 Human Fetal Brain, normalized Human Fetal Brain pCMVSport 2.0 C500H H0571 Human Fetal Brain, normalized Human Fetal Brain pCMVSport 2.0 C500HE H0572 Human Fetal Brain, normalized Human Fetal Brain pCMVSport 2.0 AC5002 H0574 Hepatocellular Tumor; re-excision Hepatocellular Tumor Liver disease Lambda ZAP II H0575 Human Adult Pulmonary; re- Human Adult Pulmonary Lung Uni-ZAP XR excision H0576 Resting T-Cell; re-excision T-Cells Blood Cell Line Lambda ZAP II H0580 Dendritic cells, pooled Pooled dendritic cells pCMVSport 3.0 H0581 Human Bone Marrow, treated Human Bone Marrow Bone pCMVSport 3.0 Marrow H0583 B Cell lymphoma B Cell Lymphoma B Cell disease pCMVSport 3.0 H0584 Activated T-cells, 24 hrs, re-excision Activated T-Cells Blood Cell Line Uni-ZAP XR H0585 Activated T-Cells, 12 hrs, re-excision Activated T-Cells Blood Cell Line Uni-ZAP XR H0586 Healing groin wound, 6.5 hours post healing groin wound, 6.5 groin disease pCMVSport 3.0 incision hours post incision-2/ H0587 Healing groin wound; 7.5 hours post Groin-Feb. 19, 1997 groin disease pCMVSport 3.0 incision H0589 CD34 positive cells (cord blood), re- CD34 Positive Cells Cord Blood ZAP Express ex H0590 Human adult small intestine, re- Human Adult Small Intestine Small Int. Uni-ZAP XR excision H0591 Human T-cell lymphoma; re- T-Cell Lymphoma T-Cell disease Uni-ZAP XR excision H0592 Healing groin wound - zero hr post- HGS wound healing project; disease pCMVSport 3.0 incision (control) abdomen H0593 Olfactory epithelium; nasalcavity Olfactory epithelium from roof of pCMVSport 3.0 left nasal cacit H0594 Human Lung Cancer; re-excision Human Lung Cancer Lung disease Lambda ZAP II H0595 Stomach cancer (human); re-excision Stomach Cancer-5383A (human) disease Uni-ZAP XR H0596 Human Colon Cancer; re-excision Human Colon Cancer Colon Lambda ZAP II H0597 Human Colon; re-excision Human Colon Lambda ZAP II H0598 Human Stomach; re-excision Human Stomach Stomach Uni-ZAP XR H0599 Human Adult Heart; re-excision Human Adult Heart Heart Uni-ZAP XR H0600 Healing Abdomen wound; 70&90 min Abdomen disease pCMVSport 3.0 post incision H0601 Healing Abdomen Wound; 15 days Abdomen disease pCMVSport 3.0 post incision H0602 Healing Abdomen Wound; 21&29 Abdomen disease pCMVSport 3.0 days post incision H0604 Human Pituitary, re-excision Human Pituitary pBLUESCRIPT ™ H0606 Human Primary Breast Cancer; re- Human Primary Breast Cancer Breast disease Uni-ZAP XR excision H0607 H. Leukocytes, normalized cot 50A3 H. Leukocytes pCMVSport 1 H0609 H. Leukocytes, normalized cot > 500A H. Leukocytes pCMVSport 1 H0611 H. Leukocytes, normalized cot 500B H. Leukocytes pCMVSport 1 H0613 H. Leukocytes, normalized cot 5B H. Leukocytes pCMVSport 1 H0614 H. Leukocytes, normalized cot 500A H. Leukocytes pCMVSport 1 H0615 Human Ovarian Cancer Reexcision Ovarian Cancer Ovary disease Uni-ZAP XR H0616 Human Testes, Reexcision Human Testes Testis Uni-ZAP XR H0617 Human Primary Breast Cancer Human Primary Breast Cancer Breast disease Uni-ZAP XR Reexcision H0618 Human Adult Testes, Large Inserts, Human Adult Testis Testis Uni-ZAP XR Reexcision H0619 Fetal Heart Human Fetal Heart Heart Uni-ZAP XR H0620 Human Fetal Kidney; Reexcision Human Fetal Kidney Kidney Uni-ZAP XR H0622 Human Pancreas Tumor; Reexcision Human Pancreas Tumor Pancreas disease Uni-ZAP XR H0623 Human Umbilical Vein; Reexcision Human Umbilical Vein Endothelial Umbilical Uni-ZAP XR Cells vein H0624 12 Week Early Stage Human II; Twelve Week Old Early Stage Embryo Uni-ZAP XR Reexcision Human H0625 Ku 812F Basophils Line Ku 812F Basophils pSport1 H0626 Saos2 Cells; Untreated Saos2 Cell Line; Untreated pSport1 H0627 Saos2 Cells; Vitamin D3 Treated Saos2 Cell Line; Vitamin D3 pSport1 Treated H0628 Human Pre-Differentiated Human Pre-Differentiated Uni-ZAP XR Adipocytes Adipocytes H0629 Human Leukocyte, control #2 Human Normalized leukocyte pCMVSport 1 H0631 Saos2, Dexamethosome Treated Saos2 Cell Line; Dexamethosome pSport1 Treated H0632 Hepatocellular Tumor; re-excision Hepatocellular Tumor Liver Lambda ZAP II H0633 Lung Carcinoma A549 TNFalpha TNFalpha activated A549--Lung disease pSport1 activated Carcinoma H0634 Human Testes Tumor, re-excision Human Testes Tumor Testis disease Uni-ZAP XR H0635 Human Activated T-Cells, re- Activated T-Cells Blood Cell Line Uni-ZAP XR excision H0637 Dendritic Cells From CD34 Cells Dentritic cells from CD34 cells pSport1 H0638 CD40 activated monocyte dendridic CD40 activated monocyte pSport1 cells dendridic cells H0640 FICOLL ™ ed Human Stromal Cells, FICOLL ™ ed Human Stromal Other Untreated Cells, Untreated H0641 LPS activated derived dendritic cells LPS activated monocyte derived pSport1 dendritic cells H0642 Hep G2 Cells, lambda library Hep G2 Cells Other H0643 Hep G2 Cells, PCR library Hep G2 Cells Other H0644 Human Placenta (re-excision) Human Placenta Placenta Uni-ZAP XR H0645 Fetal Heart, re-excision Human Fetal Heart Heart Uni-ZAP XR H0646 Lung, Cancer (4005313 A3): Metastatic squamous cell lung pSport1 Invasive Poorly Differentiated Lung carcinoma, poorly di Adenocarcinoma, H0647 Lung, Cancer (4005163 B7): Invasive poorly differentiated lung disease pSport1 Invasive, Poorly Diff. adenocarcinoma Adenocarcinoma, Metastatic H0648 Ovary, Cancer: (4004562 B6) Papillary Cstic neoplasm of low disease pSport1 Papillary Serous Cystic Neoplasm, malignant potentia Low Malignant Pot H0649 Lung, Normal: (4005313 B1) Normal Lung pSport1 H0650 B-Cells B-Cells pCMVSport 3.0 H0651 Ovary, Normal: (9805C040R) Normal Ovary pSport1 H0652 Lung, Normal: (4005313 B1) Normal Lung pSport1 H0653 Stromal Cells Stromal Cells pSport1 H0654 Lung, Cancer: (4005313 A3) Metastatic Squamous cell lung Other Invasive Poorly-differentiated Carcinoma poorly dif Metastatic lung adenoc H0656 B-cells (unstimulated) B-cells (unstimulated) pSport1 H0657 B-cells (stimulated) B-cells (stimulated) pSport1 H0658 Ovary, Cancer (9809C332): Poorly 9809C332-Poorly differentiate Ovary & disease pSport1 differentiated adenocarcinoma Fallopian Tubes H0659 Ovary, Cancer (15395A1F): Grade Grade II Papillary Carcinoma, Ovary disease pSport1 II Papillary Carcinoma Ovary H0660 Ovary, Cancer: (15799A1F) Poorly Poorly differentiated carcinoma, disease pSport1 differentiated carcinoma ovary H0661 Breast, Cancer: (4004943 A5) Breast cancer disease pSport1 H0662 Breast, Normal: (4005522B2) Normal Breast-#4005522(B2) Breast pSport1 H0663 Breast, Cancer: (4005522 A2) Breast Cancer-#4005522(A2) Breast disease pSport1 H0664 Breast, Cancer: (9806C012R) Breast Cancer Breast disease pSport1 H0665 Stromal cells 3.88 Stromal cells 3.88 pSport1 H0666 Ovary, Cancer: (4004332 A2) Ovarian Cancer, Sample disease pSport1 #4004332A2 H0667 Stromal cells(HBM3.18) Stromal cell(HBM 3.18) pSport1 H0668 stromal cell clone 2.5 stromal cell clone 2.5 pSport1 H0669 Breast, Cancer: (4005385 A2) Breast Cancer (4005385A2) Breast pSport1 H0670 Ovary, Cancer(4004650 A3): Well- Ovarian Cancer-4004650A3 pSport1 Differentiated Micropapillary Serous Carcinoma H0671 Breast, Cancer: (9802C02OE) Breast Cancer-Sample # pSport1 9802C02OE H0672 Ovary, Cancer: (4004576 A8) Ovarian Cancer(4004576A8) Ovary pSport1 H0673 Human Prostate Cancer, Stage B2; Human Prostate Cancer, stage B2 Prostate Uni-ZAP XR re-excision H0674 Human Prostate Cancer, Stage C; re- Human Prostate Cancer, stage C Prostate Uni-ZAP XR excission H0675 Colon, Cancer: (9808C064R) Colon Cancer 9808C064R pCMVSport 3.0 H0676 Colon, Cancer: (9808C064R)-total Colon Cancer 9808C064R pCMVSport 3.0 RNA H0677 TNFR degenerate oligo B-Cells PCRII H0678 screened clones from placental Placenta Placenta Other library H0682 Serous Papillary Adenocarcinoma serous papillary adenocarcinoma pCMVSport 3.0 (9606G304SPA3B) H0683 Ovarian Serous Papillary Serous papillary adenocarcinoma, pCMVSport 3.0 Adenocarcinoma stage 3C (9804G01 H0684 Serous Papillary Adenocarcinoma Ovarian Cancer-9810G606 Ovaries pCMVSport 3.0 H0685 Adenocarcinoma of Ovary, Human Adenocarcinoma of Ovary, Human pCMVSport 3.0 Cell Line, # OVCAR-3 Cell Line, # OVCAR- H0686 Adenocarcinoma of Ovary, Human Adenocarcinoma of Ovary, Human pCMVSport 3.0 Cell Line Cell Line, # SW-626 H0687 Human normal ovary(#9610G215) Human normal ovary(#9610G215) Ovary pCMVSport 3.0 H0688 Human Ovarian Human Ovarian pCMVSport 3.0 Cancer(#9807G017) cancer(#9807G017), mRNA from Maura Ru H0689 Ovarian Cancer Ovarian Cancer, #9806G019 pCMVSport 3.0 H0690 Ovarian Cancer, # 9702G001 Ovarian Cancer, #9702G001 pCMVSport 3.0 H0691 Normal Ovary, #9710G208 normal ovary, #9710G208 pCMVSport 3.0 H0693 Normal Prostate #ODQ3958EN Normal Prostate Tissue # pCMVSport 3.0 ODQ3958EN H0694 Prostate gland adenocarcinoma Prostate gland, adenocarcinoma, prostate pCMVSport 3.0 mod/diff, gleason gland H0695 mononucleocytes from patient mononucleocytes from patient at pCMVSport 3.0 Shady Grove Hospit N0003 Human Fetal Brain Human Fetal Brain N0006 Human Fetal Brain Human Fetal Brain N0007 Human Hippocampus Human Hippocampus N0009 Human Hippocampus, prescreened Human Hippocampus S0001 Brain frontal cortex Brain frontal cortex Brain Lambda ZAP II S0002 Monocyte activated Monocyte-activated blood Cell Line Uni-ZAP XR S0003 Human Osteoclastoma Osteoclastoma bone disease Uni-ZAP XR S0004 Prostate Prostate BPH Prostate Lambda ZAP II S0005 Heart Heart-left ventricle Heart pCDNA S0006 Neuroblastoma Human Neural Blastoma disease pCDNA S0007 Early Stage Human Brain Human Fetal Brain Uni-ZAP XR S0010 Human Amygdala Amygdala Uni-ZAP XR S0011 STROMAL-OSTEOCLASTOMA Osteoclastoma bone disease Uni-ZAP XR S0013 Prostate Prostate prostate Uni-ZAP XR S0014 Kidney Cortex Kidney cortex Kidney Uni-ZAP XR S0015 Kidney medulla Kidney medulla Kidney Uni-ZAP XR S0016 Kidney Pyramids Kidney pyramids Kidney Uni-ZAP XR S0021 Whole brain Whole brain Brain ZAP Express S0022 Human Osteoclastoma Stromal Cells - Osteoclastoma Stromal Cells Uni-ZAP XR unamplified S0024 Human Kidney Medulla - Human Kidney Medulla unamplified S0026 Stromal cell TF274 stromal cell Bone marrow Cell Line Uni-ZAP XR S0027 Smooth muscle, serum treated Smooth muscle Pulmanary Cell Line Uni-ZAP XR artery S0028 Smooth muscle, control Smooth muscle Pulmanary Cell Line Uni-ZAP XR artery S0029 brain stem Brain stem brain Uni-ZAP XR S0030 Brain pons Brain Pons Brain Uni-ZAP XR S0031 Spinal cord Spinal cord spinal cord Uni-ZAP XR S0032 Smooth muscle-ILb induced Smooth muscle Pulmanary Cell Line Uni-ZAP XR artery S0035 Brain medulla oblongata Brain medulla oblongata Brain Uni-ZAP XR S0036 Human Substantia Nigra Human Substantia Nigra Uni-ZAP XR S0037 Smooth muscle, IL1b induced Smooth muscle Pulmanary Cell Line Uni-ZAP XR artery S0038 Human Whole Brain #2 - Human Whole Brain #2 ZAP Express Oligo dT > 1.5 Kb S0039 Hypothalamus Hypothalamus Brain Uni-ZAP XR S0040 Adipocytes Human Adipocytes from Uni-ZAP XR Osteoclastoma S0042 Testes Human Testes ZAP Express S0044 Prostate BPH prostate BPH Prostate disease Uni-ZAP XR S0045 Endothelial cells-control Endothelial cell endothelial Cell Line Uni-ZAP XR cell-lung S0046 Endothelial-induced Endothelial cell endothelial Cell Line Uni-ZAP XR cell-lung S0048 Human Hypothalamus, Alzheimer''s Human Hypothalamus, disease Uni-ZAP XR Alzheimer''s S0049 Human Brain, Striatum Human Brain, Striatum Uni-ZAP XR S0050 Human Frontal Cortex, Human Frontal Cortex, disease Uni-ZAP XR Schizophrenia Schizophrenia S0051 Human Hypothalmus, Schizophrenia Human Hypothalamus, disease Uni-ZAP XR Schizophrenia S0052 neutrophils control human neutrophils blood Cell Line Uni-ZAP XR S0053 Neutrophils IL-1 and LPS induced human neutrophil induced blood Cell Line Uni-ZAP XR S0106 STRIATUM DEPRESSION BRAIN disease Uni-ZAP XR S0110 Brain Amygdala Depression Brain disease Uni-ZAP XR S0112 Hypothalamus Brain Uni-ZAP XR S0114 Anergic T-cell Anergic T-cell Cell Line Uni-ZAP XR S0116 Bone marrow Bone marrow Bone marrow Uni-ZAP XR S0122 Osteoclastoma-normalized A Osteoclastoma bone disease pBLUESCRIPT ™ S0124 Smooth muscle-edited A Smooth muscle Pulmanary Cell Line Uni-ZAP XR artery S0126 Osteoblasts Osteoblasts Knee Cell Line Uni-ZAP XR S0132 Epithelial-TNFa and INF induced Airway Epithelial Uni-ZAP XR S0134 Apoptotic T-cell apoptotic cells Cell Line Uni-ZAP XR S0136 PERM TF274 stromal cell Bone marrow Cell Line Lambda ZAP II S0140 eosinophil-IL5 induced eosinophil lung Cell Line Uni-ZAP XR S0142 Macrophage-oxLDL macrophage-oxidized LDL treated blood Cell Line Uni-ZAP XR S0144 Macrophage (GM-CSF treated) Macrophage (GM-CSF treated) Uni-ZAP XR S0146 prostate-edited prostate BPH Prostate Uni-ZAP XR S0148 Normal Prostate Prostate prostate Uni-ZAP XR S0150 LNCAP prostate cell line LNCAP Cell Line Prostate Cell Line Uni-ZAP XR S0152 PC3 Prostate cell line PC3 prostate cell line Uni-ZAP XR S0168 Prostate/LNCAP, subtraction I PC3 prostate cell line pBLUESCRIPT ™ S0176 Prostate, normal, subtraction I Prostate prostate Uni-ZAP XR S0180 Bone Marrow Stroma, TNF&LPS Bone Marrow Stroma, TNF & LPS disease Uni-ZAP XR ind induced S0182 Human B Cell 8866 Human B-Cell 8866 Uni-ZAP XR S0188 Prostate, BPH, Lib 2 Human Prostate BPH disease pSport1 S0190 Prostate BPH, Lib 2, subtracted Human Prostate BPH pSport1 S0192 Synovial Fibroblasts (control) Synovial Fibroblasts pSport1 S0194 Synovial hypoxia Synovial Fibroblasts pSport1 S0196 Synovial IL-1/TNF stimulated Synovial Fibroblasts pSport1 S0206 Smooth Muscle-HASTE Smooth muscle Pulmanary Cell Line pBLUESCRIPT ™ normalized artery S0208 Messangial cell, frac 1 Messangial cell pSport1 S0210 Messangial cell, frac 2 Messangial cell pSport1 S0212 Bone Marrow Stromal Cell, Bone Marrow Stromal pSport1 untreated Cell, untreated S0214 Human Osteoclastoma, re-excision Osteoclastoma bone disease Uni-ZAP XR S0216 Neutrophils IL-1 and LPS induced human neutrophil induced blood Cell Line Uni-ZAP XR S0218 Apoptotic T-cell, re-excision apoptotic cells Cell Line Uni-ZAP XR S0220 H. hypothalamus, frac A; re-excision Hypothalamus Brain ZAP Express S0222 H. Frontal cortex, epileptic; re- H. Brain, Frontal Cortex, Epileptic Brain disease Uni-ZAP XR excision S0242 Synovial Fibroblasts (Il1/TNF), subt Synovial Fibroblasts pSport1 S0250 Human Osteoblasts II Human Osteoblasts Femur disease pCMVSport 2.0 S0260 Spinal Cord, re-excision Spinal cord spinal cord Uni-ZAP XR S0276 Synovial hypoxia-RSF subtracted Synovial fobroblasts (rheumatoid) Synovial pSport1 tissue S0278 H Macrophage (GM-CSF treated), Macrophage (GM-CSF treated) Uni-ZAP XR re-excision S0280 Human Adipose Tissue, re-excision Human Adipose Tissue Uni-ZAP XR S0282 Brain Frontal Cortex, re-excision Brain frontal cortex Brain Lambda ZAP II S0292 Osteoarthritis (OA-4) Human Osteoarthritic Cartilage Bone disease pSport1 S0294 Larynx tumor Larynx tumor Larynx, vocal disease pSport1 cord S0298 Bone marrow stroma, treated Bone marrow stroma, treatedSB Bone marrow pSport1 S0300 Frontal lobe, dementia; re-excision Frontal Lobe dementia/ Brain Uni-ZAP XR Alzheimer''s S0306 Larynx normal #10 261-273 Larynx normal pSport1 S0308 Spleen/normal Spleen normal pSport1 S0310 Normal trachea Normal trachea pSport1 S0312 Human osteoarthritic; fraction II Human osteoarthritic cartilage disease pSport1 S0314 Human osteoarthritis; fraction I Human osteoarthritic cartilage disease pSport1 S0316 Human Normal Cartilage, Fraction I Human Normal Cartilage pSport1 S0318 Human Normal Cartilage Fraction II Human Normal Cartilage pSport1 S0328 Palate carcinoma Palate carcinoma Uvula disease pSport1 S0330 Palate normal Palate normal Uvula pSport1 S0332 Pharynx carcinoma Pharynx carcinoma Hypopharynx pSport1 S0334 Human Normal Cartilage Fraction Human Normal Cartilage pSport1 III S0336 Human Normal Cartilage Fraction Human Normal Cartilage pSport1 IV S0338 Human Osteoarthritic Cartilage Human osteoarthritic cartilage disease pSport1 Fraction III S0340 Human Osteoarthritic Cartilage Human osteoarthritic cartilage disease pSport1 Fraction IV S0342 Adipocytes; re-excision Human Adipocytes from Uni-ZAP XR Osteoclastoma S0344 Macrophage-oxLDL; re-excision macrophage-oxidized LDL treated blood Cell Line Uni-ZAP XR S0346 Human Amygdala; re-excision Amygdala Uni-ZAP XR S0348 Cheek Carcinoma Cheek Carcinoma disease pSport1 S0350 Pharynx Carcinoma Pharynx carcinoma Hypopharynx disease pSport1 S0352 Larynx Carcinoma Larynx carcinoma disease pSport1 S0354 Colon Normal II Colon Normal Colon pSport1 S0356 Colon Carcinoma Colon Carcinoma Colon disease pSport1 S0358 Colon Normal III Colon Normal Colon pSport1 S0360 Colon Tumor II Colon Tumor Colon disease pSport1 S0362 Human Gastrocnemius Gastrocnemius muscle pSport1 S0364 Human Quadriceps Quadriceps muscle pSport1 S0366 Human Soleus Soleus Muscle pSport1 S0368 Human Pancreatic Langerhans Islets of Langerhans pSport1 S0370 Larynx carcinoma II Larynx carcinoma disease pSport1 S0372 Larynx carcinoma III Larynx carcinoma disease pSport1 S0374 Normal colon Normal colon pSport1 S0376 Colon Tumor Colon Tumor disease pSport1 S0378 Pancreas normal PCA4 No Pancreas Normal PCA4 No pSport1 S0380 Pancreas Tumor PCA4 Tu Pancreas Tumor PCA4 Tu disease pSport1 S0382 Larynx carcinoma IV Larynx carcinoma disease pSport1 S0384 Tongue carcinoma Tongue carcinoma disease pSport1 S0386 Human Whole Brain, re-excision Whole brain Brain ZAP Express S0388 Human Human Hypothalamus, disease Uni-ZAP XR Hypothalamus, schizophrenia, re- Schizophrenia excision S0390 Smooth muscle, control; re-excision Smooth muscle Pulmanary Cell Line Uni-ZAP XR artery S0392 Salivary Gland Salivary gland; normal pSport1 S0394 Stomach; normal Stomach; normal pSport1 S0398 Testis; normal Testis; normal pSport1 S0400 Brain; normal Brain; normal pSport1 S0402 Adrenal Gland, normal Adrenal gland; normal pSport1 S0404 Rectum normal Rectum, normal pSport1 S0406 Rectum tumour Rectum tumour pSport1 S0408 Colon, normal Colon, normal pSport1 S0410 Colon, tumour Colon, tumour pSport1 S0412 Temporal cortex-Alzheizmer; Temporal cortex, alzheimer disease Other subtracted S0414 Hippocampus, Alzheimer Subtracted Hippocampus, Alzheimer Other Subtracted S0418 CHME Cell Line; treated 5 hrs CHME Cell Line; treated pCMVSport 3.0 S0420 CHME Cell Line, untreated CHME Cell line, untreatetd pSport1 S0422 Mo7e Cell Line GM-CSF treated Mo7e Cell Line GM-CSF treated pCMVSport 3.0 (1 ng/ml) (1 ng/ml) S0424 TF-1 Cell Line GM-CSF Treated TF-1 Cell Line GM-CSF Treated pSport1 S0426 Monocyte activated; re-excision Monocyte-activated blood Cell Line Uni-ZAP XR S0428 Neutrophils control; re-excision human neutrophils blood Cell Line Uni-ZAP XR S0430 Aryepiglottis Normal Aryepiglottis Normal pSport1 S0432 Sinus piniformis Tumour Sinus piniformis Tumour pSport1 S0434 Stomach Normal Stomach Normal disease pSport1 S0436 Stomach Tumour Stomach Tumour disease pSport1 S0438 Liver Normal Met5No Liver Normal Met5No pSport1 S0440 Liver Tumour Met 5 Tu Liver Tumour pSport1 S0442 Colon Normal Colon Normal pSport1 S0444 Colon Tumor Colon Tumour disease pSport1 S0446 Tongue Tumour Tongue Tumour pSport1 S0448 Larynx Normal Larynx Normal pSport1 S0450 Larynx Tumour Larynx Tumour pSport1 S0452 Thymus Thymus pSport1 S0454 Placenta Placenta Placenta pSport1 S0456 Tongue Normal Tongue Normal pSport1 S0458 Thyroid Normal (SDCA2 No) Thyroid normal pSport1 S0460 Thyroid Tumour Thyroid Tumour pSport1 S0462 Thyroid Thyroiditis Thyroid Thyroiditis pSport1 S0464 Larynx Normal Larynx Normal pSport1 S0466 Larynx Tumor Larynx Tumor disease pSport1 S0468 Ea.hy.926 cell line Ea.hy.926 cell line pSport1 S0470 Adenocarcinoma PYFD disease pSport1 S0472 Lung Mesothelium PYBT pSport1 S0474 Human blood platelets Platelets Blood Other platelets S0665 Human Amygdala; re-excission Amygdala Uni-ZAP XR S3012 Smooth Muscle Serum Treated, Smooth muscle Pulmanary Cell Line pBLUESCRIPT ™ Norm artery S3014 Smooth muscle, serum induced, re- Smooth muscle Pulmanary Cell Line pBLUESCRIPT ™ exc artery S6014 H. hypothalamus, frac A Hypothalamus Brain ZAP Express S6016 H. Frontal Cortex, Epileptic H. Brain, Frontal Cortex, Epileptic Brain disease Uni-ZAP XR S6022 H. Adipose Tissue Human Adipose Tissue Uni-ZAP XR S6024 Alzheimers, spongy change Alzheimer''s/Spongy change Brain disease Uni-ZAP XR S6026 Frontal Lobe, Dementia Frontal Lobe dementia/ Brain Uni-ZAP XR Alzheimer''s S6028 Human Manic Depression Tissue Human Manic depression tissue Brain disease Uni-ZAP XR T0002 Activated T-cells Activated T-Cell, PBL fraction Blood Cell Line pBLUESCRIPT ™ SK− T0003 Human Fetal Lung Human Fetal Lung pBLUESCRIPT ™ SK− T0004 Human White Fat Human White Fat pBLUESCRIPT ™ SK− T0006 Human Pineal Gland Human Pinneal Gland pBLUESCRIPT ™ SK− T0007 Colon Epithelium Colon Epithelium pBLUESCRIPT ™ I SK− T0008 Colorectal Tumor Colorectal Tumor disease pBLUESCRIPT ™ SK− T0010 Human Infant Brain Human Infant Brain Other T0023 Human Pancreatic Carcinoma Human Pancreatic Carcinoma disease pBLUESCRIPT ™ SK− T0039 HSA 172 Cells Human HSA172 cell line pBLUESCRIPT ™ SK− T0040 HSC172 cells SA172 Cells pBLUESCRIPT ™ SK− T0041 Jurkat T-cell G1 phase Jurkat T-cell pBLUESCRIPT ™ SK− T0042 Jurkat T-Cell, S phase Jurkat T-Cell Line pBLUESCRIPT ™ SK− T0048 Human Aortic Endothelium Human Aortic Endothilium pBLUESCRIPT ™ SK− T0049 Aorta endothelial cells + TNF-a Aorta endothelial cells pBLUESCRIPT ™ SK− T0060 Human White Adipose Human White Fat pBLUESCRIPT ™ SK− T0067 Human Thyroid Human Thyroid pBLUESCRIPT ™ SK− T0068 Normal Ovary, Premenopausal Normal Ovary, Premenopausal pBLUESCRIPT ™ SK− T0069 Human Uterus, normal Human Uterus, normal pBLUESCRIPT ™ SK− T0071 Human Bone Marrow Human Bone Marrow pBLUESCRIPT ™ SK− T0079 Human Kidney, normal Adult Human Kidney, normal Adult pBLUESCRIPT ™ SK− T0082 Human Adult Retina Human Adult Retina pBLUESCRIPT ™ SK− T0086 Human Pancreatic Carcinoma - Human Pancreatic Carcinoma disease pBLUESCRIPT ™ Screened SK− T0087 Alzheimer''s, exon trap, 712P disease pAMP T0103 Human colon carcinoma (HCC) cell pBLUESCRIPT ™ line SK− T0104 HCC cell line metastisis to liver pBLUESCRIPT ™ SK− T0109 Human (HCC) cell line liver pBLUESCRIPT ™ (mouse) metastasis, remake SK− T0110 Human colon carcinoma (HCC) cell pBLUESCRIPT ™ line, remake SK− T0112 Human (Caco-2) cell line, pBLUESCRIPT ™ adenocarcinoma, colon SK− T0114 Human (Caco-2) cell line, pBLUESCRIPT ™ adenocarcinoma, colon, remake SK− T0115 Human Colon Carcinoma (HCC) pBLUESCRIPT ™ cell line SK− L0002 Atrium cDNA library Human heart L0005 CLONTECH ™ human aorta polyA + mRNA (#6572) L0015 Human L0021 Human adult (K. Okubo) L0022 Human adult lung 3″ directed MboI cDNA L0024 Human brain ARSanders L0040 Human colon mucosa L0041 Human epidermal keratinocyte L0045 Human keratinocyte differential display (B. Lin) L0053 Human pancreatic tumor L0055 Human promyelocyte L0065 Liver HepG2 cell line. L0096 Subtracted human retina L0097 Subtracted human retinal pigment epithelium (RPE) L0103 DKFZphamy1 amygdala L0105 Human aorta polyA+ (TFujiwara) aorta L0142 Human placenta cDNA (TFujiwara) placenta L0143 Human placenta polyA+ placenta (TFujiwara) L0151 Human testis (C. De Smet) testis L0157 Human fetal brain (TFujiwara) brain L0163 Human heart cDNA (YNakamura) heart L0182 Human HeLa (Y. Wang) HeLa L0187 Human fibrosarcoma cell line fibrosarcoma HT1080 HT1080 L0194 Human pancreatic cancer cell line pancreatic cancer Patu Patu 8988t 8988t L0295 Human liver EST (Y. L. Yu) liver L0309 Human E8CASS breast adenocarcinoma E8CASS; variant of MCF7 L0351 Infant brain, Bento Soares BA, M13-derived L0352 Normalized infant brain, Bento BA, M13-derived Soares L0355 P, Human foetal Brain Whole tissue Bluescript L0356 S, Human foetal Adrenals tissue Bluescript L0361 STRATAGENE ™ ovary (#937217) ovary Bluescript SK L0362 STRATAGENE ™ ovarian cancer Bluescript SK− (#937219) L0363 NCI_CGAP_GC2 germ cell tumor Bluescript SK− L0364 NCI_CGAP_GC5 germ cell tumor Bluescript SK− L0365 NCI_CGAP_Phe1 pheochromocytoma Bluescript SK− L0366 STRATAGENE ™ schizo brain S11 schizophrenic brain S-11 frontal Bluescript SK− lobe L0367 NCI_CGAP_Sch1 Schwannoma tumor Bluescript SK− L0368 NCI_CGAP_SS1 synovial sarcoma Bluescript SK− L0369 NCI_CGAP_AA1 adrenal adenoma adrenal gland Bluescript SK− L0370 Johnston frontal cortex pooled frontal lobe brain Bluescript SK− L0371 NCI_CGAP_Br3 breast tumor breast Bluescript SK− L0372 NCI_CGAP_Co12 colon tumor colon Bluescript SK− L0373 NCI_CGAP_Co11 tumor colon Bluescript SK− L0374 NCI_CGAP_Co2 tumor colon Bluescript SK− L0375 NCI_CGAP_Kid6 kidney tumor kidney Bluescript SK− L0376 NCI_CGAP_Lar1 larynx larynx Bluescript SK− L0378 NCI_CGAP_Lu1 lung tumor lung Bluescript SK− L0379 NCI_CGAP_Lym3 lymphoma lymph node Bluescript SK− L0381 NCI_CGAP_HN4 squamous cell carcinoma pharynx Bluescript SK− L0382 NCI_CGAP_Pr25 epithelium (cell line) prostate Bluescript SK− L0383 NCI_CGAP_Pr24 invasive tumor (cell line) prostate Bluescript SK− L0384 NCI_CGAP_Pr23 prostate tumor prostate Bluescript SK− L0385 NCI_CGAP_Gas1 gastric tumor stomach Bluescript SK− L0386 NCI_CGAP_HN3 squamous cell carcinoma tongue Bluescript SK− from base of tongue L0387 NCI_CGAP_GCB0 germinal center B-cells tonsil Bluescript SK− L0388 NCI_CGAP_HN6 normal gingiva (cell line from Bluescript SK− immortalized kerati L0389 NCI_CGAP_HN5 normal gingiva (cell line from Bluescript SK− primary keratinocyt L0394 H, Human adult Brain Cortex tissue gt11 L0404 b4HB3MA Cot109 + 103 + 85-Bio Lafmid A L0411 1-NIB Lafmid BA L0415 b4HB3MA Cot8-HAP-Ft Lafmid BA L0418 b4HB3MA-Cot109 + 10-Bio Lafmid BA L0428 Cot1374Ft-4HB3MA Lafmid BA L0435 Infant brain, LLNL array of Dr. lafmid BA M. Soares 1NIB L0438 normalized infant brain cDNA total brain brain lafmid BA L0439 Soares infant brain 1NIB whole brain Lafmid BA L0446 N4HB3MK Lafmid BK L0455 Human retina cDNA randomly retina eye lambda gt10 primed sublibrary L0456 Human retina cDNA Tsp509I- retina eye lambda gt10 cleaved sublibrary L0457 multi-tissue normalized short- multi-tissue pooled lambda gt10 fragment L0459 Adult heart, CLONTECH ™ Lambda gt11 L0460 Adult heart, Lambda gt11 Lambda gt11 L0462 WATM1 lambda gt11 L0463 fetal brain cDNA brain brain lambda gt11 L0465 TEST1, Human adult Testis tissue lambda nm1149 L0471 Human fetal heart, Lambda ZAP Lambda ZAP Express Express L0475 KG1-a Lambda Zap Express cDNA KG1-a Lambda Zap library Express (STRATAGENE ™) L0476 Fetal brain, STRATAGENE ™ Lambda ZAP II L0480 STRATAGENE ™ cat#937212 Lambda ZAP, (1992) pBLUESCRIPT ™ SK(−) L0481 CD34 + DIRECTIONAL Lambda ZAPII L0483 Human pancreatic islet Lambda ZAPII L0485 STRATAGENE ™ Human skeletal skeletal muscle leg muscle Lambda ZAPII muscle cDNA library, cat. #936215. L0492 Human Genomic pAMP L0493 NCI_CGAP_Ov26 papillary serous carcinoma ovary pAMP1 L0497 NCI_CGAP_HSC4 CD34+, CD38− from normal bone bone marrow pAMP1 marrow donor L0498 NCI_CGAP_HSC3 CD34+, T negative, patient with bone marrow pAMP1 chronic myelogenou L0499 NCI_CGAP_HSC2 stem cell 34+/38+ bone marrow pAMP1 L0500 NCI_CGAP_Brn20 oligodendroglioma brain pAMP1 L0502 NCI_CGAP_Br15 adenocarcinoma breast pAMP1 L0503 NCI_CGAP_Br17 adenocarcinoma breast pAMP1 L0504 NCI_CGAP_Br13 breast carcinoma in situ breast pAMP1 L0505 NCI_CGAP_Br12 invasive carcinoma breast pAMP1 L0506 NCI_CGAP_Br16 lobullar carcinoma in situ breast pAMP1 L0507 NCI_CGAP_Br14 normal epithelium breast pAMP1 L0508 NCI_CGAP_Lu25 bronchioalveolar carcinoma lung pAMP1 L0509 NCI_CGAP_Lu26 invasive adenocarcinoma lung pAMP1 L0512 NCI_CGAP_Ov36 borderline ovarian carcinoma ovary pAMP1 L0513 NCI_CGAP_Ov37 early stage papillary serous ovary pAMP1 carcinoma L0514 NCI_CGAP_Ov31 papillary serous carcinoma ovary pAMP1 L0515 NCI_CGAP_Ov32 papillary serous carcinoma ovary pAMP1 L0517 NCI_CGAP_Pr1 pAMP10 L0518 NCI_CGAP_Pr2 pAMP10 L0519 NCI_CGAP_Pr3 pAMP10 L0520 NCI_CGAP_Alv1 alveolar rhabdomyosarcoma pAMP10 L0521 NCI_CGAP_Ew1 Ewing''s sarcoma pAMP10 L0522 NCI_CGAP_Kid1 kidney pAMP10 L0523 NCI_CGAP_Lip2 liposarcoma pAMP10 L0524 NCI_CGAP_Li1 liver pAMP10 L0525 NCI_CGAP_Li2 liver pAMP10 L0526 NCI_CGAP_Pr12 metastatic prostate bone lesion pAMP10 L0527 NCI_CGAP_Ov2 ovary pAMP10 L0528 NCI_CGAP_Pr5 prostate pAMP10 L0529 NCI_CGAP_Pr6 prostate pAMP10 L0530 NCI_CGAP_Pr8 prostate pAMP10 L0532 NCI_CGAP_Thy1 thyroid pAMP10 L0533 NCI_CGAP_HSC1 stem cells bone marrow pAMP10 L0534 Chromosome 7 Fetal Brain cDNA brain brain pAMP10 Library L0539 Chromosome 7 Placental cDNA placenta pAMP10 Library L0540 NCI_CGAP_Pr10 invasive prostate tumor prostate pAMP10 L0542 NCI_CGAP_Pr11 normal prostatic epithelial cells prostate pAMP10 L0543 NCI_CGAP_Pr9 normal prostatic epithelial cells prostate pAMP10 L0544 NCI_CGAP_Pr4 prostatic intraepithelial prostate pAMP10 neoplasia - high grade L0545 NCI_CGAP_Pr4.1 prostatic intraepithelial prostate pAMP10 neoplasia - high grade L0546 NCI_CGAP_Pr18 stroma prostate pAMP10 L0547 NCI_CGAP_Pr16 tumor prostate pAMP10 L0549 NCI_CGAP_HN10 carcinoma in situ from retromolar pAMP10 trigone L0550 NCI_CGAP_HN9 normal squamous epithelium from pAMP10 retromolar trigone L0551 NCI_CGAP_HN7 normal squamous epithelium, floor pAMP10 of mouth L0553 NCI_CGAP_Co22 colonic adenocarcinoma colon pAMP10 L0554 NCI_CGAP_Li8 liver pAMP10 L0558 NCI_CGAP_Ov40 endometrioid ovarian metastasis ovary pAMP10 L0559 NCI_CGAP_Ov39 papillary serous ovarian metastasis ovary pAMP10 L0560 NCI_CGAP_HN12 moderate to poorly differentiated tongue pAMP10 invasive carcino L0561 NCI_CGAP_HN11 normal squamous epithelium tongue pAMP10 L0562 Chromosome 7 HeLa cDNA Library HeLa cell pAMP10 line; ATCC ™ L0564 Jia bone marrow stroma bone marrow stroma pBLUESCRIPT ™ L0565 Normal Human Trabecular Bone Bone Hip pBLUESCRIPT ™ Cells L0581 STRATAGENE ™ liver (#937224) liver pBLUESCRIPT ™ SK L0584 STRATAGENE ™ cDNA library pBLUESCRIPT ™ Human heart, cat#936208 SK(+) L0586 HTCDL1 pBLUESCRIPT ™ SK(−) L0587 STRATAGENE ™ colon HT29 pBLUESCRIPT ™ (#937221) SK− L0588 STRATAGENE ™ endothelial cell pBLUESCRIPT ™ 937223 SK− L0589 STRATAGENE ™ fetal retina pBLUESCRIPT ™ 937202 SK− L0590 STRATAGENE ™ fibroblast pBLUESCRIPT ™ (#937212) SK− L0591 STRATAGENE ™ HeLa cell s3 pBLUESCRIPT ™ 937216 SK− L0592 STRATAGENE ™ hNT neuron pBLUESCRIPT ™ (#937233) SK− L0593 STRATAGENE ™ neuroepithelium pBLUESCRIPT ™ (#937231) SK− L0594 STRATAGENE ™ neuroepithelium pBLUESCRIPT ™ NT2RAMI 937234 SK− L0595 STRATAGENE ™ NT2 neuronal neuroepithelial cells brain pBLUESCRIPT ™ precursor 937230 SK− L0596 STRATAGENE ™ colon (#937204) colon pBLUESCRIPT ™ SK− L0597 STRATAGENE ™ corneal stroma cornea pBLUESCRIPT ™ (#937222) SK− L0598 Morton Fetal Cochlea cochlea ear pBLUESCRIPT ™ SK− L0599 STRATAGENE ™ lung (#937210) lung pBLUESCRIPT ™ SK− L0600 Weizmann Olfactory Epithelium olfactory epithelium nose pBLUESCRIPT ™ SK− L0601 STRATAGENE ™ pancreas pancreas pBLUESCRIPT ™ (#937208) SK− L0602 Pancreatic Islet pancreatic islet pancreas pBLUESCRIPT ™ SK− L0603 STRATAGENE ™ placenta placenta pBLUESCRIPT ™ (#937225) SK− L0604 STRATAGENE ™ muscle 937209 muscle skeletal pBLUESCRIPT ™ muscle SK− L0605 STRATAGENE ™ fetal spleen fetal spleen spleen pBLUESCRIPT ™ (#937205) SK− L0606 NCI_CGAP_Lym5 follicular lymphoma lymph node pBLUESCRIPT ™ SK− L0607 NCI_CGAP_Lym6 mantle cell lymphoma lymph node pBLUESCRIPT ™ SK− L0608 STRATAGENE ™ lung carcinoma lung carcinoma lung NCI-H69 pBLUESCRIPT ™ 937218 SK− L0609 Schiller astrocytoma astrocytoma brain pBLUESCRIPT ™ SK− (STRATAGENE ™) L0610 Schiller glioblastoma multiforme glioblastoma multiforme brain pBLUESCRIPT ™ SK− (STRATAGENE ™) L0611 Schiller meningioma meningioma brain pBLUESCRIPT ™ SK− (STRATAGENE ™) L0612 Schiller oligodendroglioma oligodendroglioma brain pBLUESCRIPT ™ SK− (STRATAGENE ™) L0615 22 week old human fetal liver pBLUESCRIPT ™ II cDNA library SK(−) L0619 Chromosome 9 exon II pBLUESCRIPT ™ II KS+ L0622 HM1 pcDNAII (Invitrogen) L0623 HM3 pectoral muscle (after mastectomy) pcDNAII (Invitrogen) L0625 NCI_CGAP_AR1 bulk alveolar tumor pCMV-SPORT2 L0626 NCI_CGAP_GC1 bulk germ cell seminoma pCMV-SPORT2 L0627 NCI_CGAP_Co1 bulk tumor colon pCMV-SPORT2 L0628 NCI_CGAP_Ov1 ovary bulk tumor ovary pCMV-SPORT2 L0629 NCI_CGAP_Me13 metastatic melanoma to bowel bowel (skin pCMV-SPORT4 primary) L0630 NCI_CGAP_CNS1 substantia nigra brain pCMV-SPORT4 L0631 NCI_CGAP_Br7 breast pCMV-SPORT4 L0634 NCI_CGAP_Ov8 serous adenocarcinoma ovary pCMV-SPORT4 L0635 NCI_CGAP_PNS1 dorsal root ganglion peripheral pCMV-SPORT4 nervous system L0636 NCI_CGAP_Pit1 four pooled pituitary adenomas brain pCMV-SPORT6 L0637 NCI_CGAP_Brn53 three pooled meningiomas brain pCMV-SPORT6 L0638 NCI_CGAP_Brn35 tumor, 5 pooled (see description) brain pCMV-SPORT6 L0639 NCI_CGAP_Brn52 tumor, 5 pooled (see description) brain pCMV-SPORT6 L0640 NCI_CGAP_Br18 four pooled high-grade tumors, breast pCMV-SPORT6 including two prima L0641 NCI_CGAP_Co17 juvenile granulosa tumor colon pCMV-SPORT6 L0642 NCI_CGAP_Co18 moderately differentiated colon pCMV-SPORT6 adenocarcinoma L0643 NCI_CGAP_Co19 moderately differentiated colon pCMV-SPORT6 adenocarcinoma L0644 NCI_CGAP_Co20 moderately differentiated colon pCMV-SPORT6 adenocarcinoma L0645 NCI_CGAP_Co21 moderately differentiated colon pCMV-SPORT6 adenocarcinoma L0646 NCI_CGAP_Co14 moderately-differentiated colon pCMV-SPORT6 adenocarcinoma L0647 NCI_CGAP_Sar4 five pooled sarcomas, including connective pCMV-SPORT6 myxoid liposarcoma tissue L0648 NCI_CGAP_Eso2 squamous cell carcinoma esophagus pCMV-SPORT6 L0649 NCI_CGAP_GU1 2 pooled high-grade transitional genitourinary pCMV-SPORT6 cell tumors tract L0650 NCI_CGAP_Kid13 2 pooled Wilms'' tumors, one kidney pCMV-SPORT6 primary and one metast L0651 NCI_CGAP_Kid8 renal cell tumor kidney pCMV-SPORT6 L0652 NCI_CGAP_Lu27 four pooled poorly-differentiated lung pCMV-SPORT6 adenocarcinomas L0653 NCI_CGAP_Lu28 two pooled squamous cell lung pCMV-SPORT6 carcinomas L0654 NCI_CGAP_Lu31 lung, cell line pCMV-SPORT6 L0655 NCI_CGAP_Lym12 lymphoma, follicular mixed small lymph node pCMV-SPORT6 and large cell L0656 NCI_CGAP_Ov38 normal epithelium ovary pCMV-SPORT6 L0657 NCI_CGAP_Ov23 tumor, 5 pooled (see description) ovary pCMV-SPORT6 L0658 NCI_CGAP_Ov35 tumor, 5 pooled (see description) ovary pCMV-SPORT6 L0659 NCI_CGAP_Pan1 adenocarcinoma pancreas pCMV-SPORT6 L0661 NCI_CGAP_Mel15 malignant melanoma, metastatic to skin pCMV-SPORT6 lymph node L0662 NCI_CGAP_Gas4 poorly differentiated stomach pCMV-SPORT6 adenocarcinoma with signet r L0663 NCI_CGAP_Ut2 moderately-differentiated uterus pCMV-SPORT6 endometrial adenocarcino L0664 NCI_CGAP_Ut3 poorly-differentiated endometrial uterus pCMV-SPORT6 adenocarcinoma, L0665 NCI_CGAP_Ut4 serous papillary carcinoma, high uterus pCMV-SPORT6 grade, 2 pooled t L0666 NCI_CGAP_Ut1 well-differentiated endometrial uterus pCMV-SPORT6 adenocarcinoma, 7 L0667 NCI_CGAP_CML1 myeloid cells, 18 pooled CML whole blood pCMV-SPORT6 cases, BCR/ABL rearra L0686 Stanley Frontal SN pool 2 frontal lobe (see description) brain pCR2.1-TOPO (Invitrogen) L0690 Testis, Subtracted pCRII L0697 Testis 1 PGEM 5zf(+) L0698 Testis 2 PGEM 5zf(+) L0708 NIH_MGC_17 rhabdomyosarcoma muscle pOTB7 L0709 NIH_MGC_21 choriocarcinoma placenta pOTB7 L0710 NIH_MGC_7 small cell carcinoma lung MGC3 pOTB7 L0717 Gessler Wilms tumor pSPORT1 L0731 Soares_pregnant_uterus_NbHPU uterus pT7T3-Pac L0738 Human colorectal cancer pT7T3D L0740 Soares melanocyte 2NbHM melanocyte pT7T3D (PHARMACIA ™) with a modified polylinker L0741 Soares adult brain N2b4HB55Y brain pT7T3D (PHARMACIA ™) with a modified polylinker L0742 Soares adult brain N2b5HB55Y brain pT7T3D (PHARMACIA ™) with a modified polylinker L0743 Soares breast 2NbHBst breast pT7T3D (PHARMACIA ™) with a modified polylinker L0744 Soares breast 3NbHBst breast pT7T3D (PHARMACIA ™) with a modified polylinker L0745 Soares retina N2b4HR retina eye pT7T3D (PHARMACIA ™) with a modified polylinker L0746 Soares retina N2b5HR retina eye pT7T3D (PHARMACIA ™) with a modified polylinker L0747 Soares_fetal_heart_NbHH19W heart pT7T3D (PHARMACIA ™) with a modified polylinker L0748 Soares fetal liver spleen 1NFLS Liver and pT7T3D Spleen (PHARMACIA ™) with a modified polylinker L0749 Soares_fetal_liver_spleen_(—) Liver and pT7T3D 1NFLS_S1 Spleen (PHARMACIA ™) with a modified polylinker L0750 Soares_fetal_lung_NbHL19W lung pT7T3D (PHARMACIA ™) with a modified polylinker L0751 Soares ovary tumor NbHOT ovarian tumor ovary pT7T3D (PHARMACIA ™) with a modified polylinker L0752 Soares_parathyroid_tumor_NbHPA parathyroid tumor parathyroid pT7T3D gland (PHARMACIA ™) with a modified polylinker L0753 Soares_pineal_gland_N3HPG pineal gland pT7T3D (PHARMACIA ™) with a modified polylinker L0754 Soares placenta Nb2HP placenta pT7T3D (PHARMACIA ™) with a modified polylinker L0755 Soares_placenta_8to9weeks_(—) placenta pT7T3D 2NbHP8to9W (PHARMACIA ™) with a modified polylinker L0756 Soares_multiple_sclerosis_2NbHMSP multiple sclerosis lesions pT7T3D (PHARMACIA ™) with a modified polylinker V_TYPE L0757 Soares_senescent_fibroblasts_NbHSF senescent fibroblast pT7T3D (PHARMACIA ™) with a modified polylinker V_TYPE L0758 Soares_testis_NHT pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0759 Soares_total_fetus_Nb2HF8_9w pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0760 Barstead aorta HPLRB3 aorta pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0761 NCI_CGAP_CLL1 B-cell, chronic lymphotic leukemia pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0762 NCI_CGAP_Br1.1 breast pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0763 NCI_CGAP_Br2 breast pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0764 NCI_CGAP_Co3 colon pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0765 NCI_CGAP_Co4 colon pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0766 NCI_CGAP_GCB1 germinal center B cell pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0767 NCI_CGAP_GC3 pooled germ cell tumors pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0768 NCI_CGAP_GC4 pooled germ cell tumors pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0769 NCI_CGAP_Brn25 anaplastic oligodendroglioma brain pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0770 NCI_CGAP_Brn23 glioblastoma (pooled) brain pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0771 NCI_CGAP_Co8 adenocarcinoma colon pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0772 NCI_CGAP_Co10 colon tumor RER+ colon pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0773 NCI_CGAP_Co9 colon tumor RER+ colon pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0774 NCI_CGAP_Kid3 kidney pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0775 NCI_CGAP_Kid5 2 pooled tumors (clear cell type) kidney pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0776 NCI_CGAP_Lu5 carcinoid lung pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0777 Soares_NhHMPu_S1 Pooled human melanocyte, fetal mixed (see pT7T3D-Pac heart, and pregnant below) (PHARMACIA ™) with a modified polylinker L0778 Barstead pancreas HPLRB1 pancreas pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0779 Soares_NFL_T_GBC_S1 pooled pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0780 Soares_NSF_F8_9W_OT_PA_(—) pooled pT7T3D-Pac P_S1 (PHARMACIA ™) with a modified polylinker L0782 NCI_CGAP_Pr21 normal prostate prostate pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0783 NCI_CGAP_Pr22 normal prostate prostate pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0784 NCI_CGAP_Lei2 leiomyosarcoma soft tissue pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0785 Barstead spleen HPLRB2 spleen pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0786 Soares_NbHFB whole brain pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0787 NCI_CGAP_Sub1 pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0788 NCI_CGAP_Sub2 pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0789 NCI_CGAP_Sub3 pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0790 NCI_CGAP_Sub4 pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0791 NCI_CGAP_Sub5 pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0792 NCI_CGAP_Sub6 pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0793 NCI_CGAP_Sub7 pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0794 NCI_CGAP_GC6 pooled germ cell tumors pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0796 NCI_CGAP_Brn50 medulloblastoma brain pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0800 NCI_CGAP_Co16 colon tumor, RER+ colon pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0803 NCI_CGAP_Kid11 kidney pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0804 NCI_CGAP_Kid12 2 pooled tumors (clear cell type) kidney pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0805 NCI_CGAP_Lu24 carcinoid lung pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0806 NCI_CGAP_Lu19 squamous cell carcinoma, poorly lung pT7T3D-Pac differentiated (4 (PHARMACIA ™) with a modified polylinker L0807 NCI_CGAP_Ov18 fibrotheoma ovary pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0808 Barstead prostate BPH HPLRB4 1 prostate pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0809 NCI_CGAP_Pr28 prostate pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L0879 BT0254 breast puc18 L0946 BT0333 breast puc18 L1057 BT0559 breast puc18 L1441 CT0249 colon puc18 L1446 CT0254 colon puc18 L1499 CT0322 colon puc18 L1788 HT0229 head_neck puc18 L1819 HT0268 head_neck puc18 L1877 HT0340 head_neck puc18 L1878 HT0342 head_neck puc18 L2138 ST0186 stomach puc18 L2174 ST0240 stomach puc18 L2251 Human fetal lung Fetal lung L2252 Human placenta placenta L2255 GLC corresponding non cancerous liver pBLUESCRIPT ™ tissue sk(- ) L2257 NIH_MGC_65 adenocarcinoma colon pCMV-SPORT6 L2258 NIH_MGC_67 retinoblastoma eye pCMV-SPORT6 L2259 NIH_MGC_68 large cell carcinoma lung pCMV-SPORT6 L2260 NIH_MGC_69 large cell carcinoma, lung pCMV-SPORT6 undifferentiated L2261 NIH_MGC_70 epithelioid carcinoma pancreas pCMV-SPORT6 L2262 NIH_MGC_72 melanotic melanoma skin pCMV-SPORT6 L2263 NIH_MGC_66 adenocarcinoma ovary pCMV-SPORT6 L2264 NIH_MGC_71 leiomyosarcoma uterus pCMV-SPORT6 L2265 NIH_MGC_39 adenocarcinoma pancreas pOTB7 L2270 Lupski_dorsal_root_ganglion dorsal root ganglia pCMV-SPORT6 (LIFE TECHNOLOGIES ™) L2289 BT0757 breast puc18 L2333 CT0417 colon puc18 L2338 CT0432 colon puc18 L2346 CT0483 colon puc18 L2357 UT0021 uterus_tumor puc18 L2367 UT0039 uterus_tumor puc18 L2377 NN0054 nervous_normal puc18 L2380 NN0068 nervous_normal puc18 L2400 NN0116 nervous_normal puc18 L2412 NN0136 nervous_normal puc18 L2413 NN0141 nervous_normal puc18 L2439 NN1022 nervous_normal puc18 L2440 NN1023 nervous_normal puc18 L2491 HT0559 head_neck puc18 L2495 HT0594 head_neck puc18 L2497 HT0618 head_neck puc18 L2504 HT0636 head_neck puc18 L2518 HT0697 head_neck puc18 L2519 HT0698 head_neck puc18 L2522 HT0704 head_neck puc18 L2539 HT0727 head_neck puc18 L2540 HT0728 head_neck puc18 L2543 HT0734 head_neck puc18 L2550 HT0743 head_neck puc18 L2570 HT0771 head_neck puc18 L2598 HT0809 head_neck puc18 L2634 HT0872 head_neck puc18 L2637 HT0877 head_neck puc18 L2640 HT0881 head_neck puc18 L2647 HT0894 head_neck puc18 L2650 HT0934 head_neck puc18 L2651 NIH_MGC_20 melanotic melanoma skin pOTB7 L2653 NIH_MGC_58 hypernephroma kidney pDNR-LIB (CLONTECH ™) L2654 NIH_MGC_9 adenocarcinoma cell line ovary pOTB7 L2655 NIH_MGC_55 from acute myelogenous leukemia bone marrow pDNR-LIB (CLONTECH ™) L2657 NIH_MGC_54 from chronic myelogenous bone marrow pDNR-LIB leukemia (CLONTECH ™) L2667 NT0013 nervous_tumor puc18 L2669 NT0022 nervous_tumor puc18 L2670 NT0023 nervous_tumor puc18 L2671 NT0024 nervous_tumor puc18 L2677 NT0039 nervous_tumor puc18 L2686 NT0058 nervous_tumor puc18 L2702 NT0098 nervous_tumor puc18 L2708 NT0104 nervous_tumor puc18 L2709 NT0105 nervous_tumor puc18 L2716 NT0117 nervous_tumor puc18 L2738 GN0049 placenta_normal puc18 L2767 FT0044 prostate_tumor puc18 L2791 FT0077 prostate_tumor puc18 L2799 FT0096 prostate_tumor puc18 L2804 FT0103 prostate_tumor puc18 L2817 FT0131 prostate_tumor puc18 L2831 FT0162 prostate_tumor puc18 L2842 UM0009 uterus puc18 L2852 UM0077 uterus puc18 L2865 AN0004 amnion_normal puc18 L2877 AN0027 amnion_normal puc18 L2884 AN0041 amnion_normal puc18 L2902 BN0036 breast_normal puc18 L2904 BN0042 breast_normal puc18 L2905 BN0046 breast_normal puc18 L2906 BN0047 breast_normal puc18 L2910 BN0070 breast_normal puc18 L2915 BN0098 breast_normal puc18 L2919 BN0115 breast_normal puc18 L2962 BN0221 breast_normal puc18 L2991 BN0264 breast_normal puc18 L2999 BN0273 breast_normal puc18 L3002 BN0276 breast_normal puc18 L3019 BN0303 breast_normal puc18 L3071 EN0026 lung_normal puc18 L3089 ET0018 lung_tumor puc18 L3104 ET0041 lung_tumor puc18 L3111 ET0058 lung_tumor puc18 L3117 ET0068 lung_tumor puc18 L3118 ET0070 lung_tumor puc18 L3119 ET0072 lung_tumor puc18 L3127 ET0084 lung_tumor puc18 L3140 MT0031 marrow puc18 L3153 MT0049 marrow puc18 L3199 OT0019 ovary puc18 L3204 OT0034 ovary puc18 L3207 OT0063 ovary puc18 L3210 OT0067 ovary puc18 L3215 OT0083 ovary puc18 L3216 OT0086 ovary puc18 L3226 FN0019 prostate_normal puc18 L3262 FN0073 prostate_normal puc18 L3281 FN0107 prostate_normal puc18 L3311 FN0180 prostate_normal puc18 L3316 FN0188 prostate_normal puc18 L3327 SN0024 stomach_normal puc18 L3330 SN0041 stomach_normal puc18 L3352 TN0027 testis_normal puc18 L3357 TN0034 testis_normal puc18 L3372 TN0068 testis_normal puc18 L3374 TN0070 testis_normal puc18 L3377 TN0079 testis_normal puc18 L3387 GKB hepatocellular carcinoma pBLUESCRIPT ™ sk(−) L3388 GKC hepatocellular carcinoma pBLUESCRIPT ™ sk(−) L3391 NIH_MGC_53 carcinoma, cell line bladder pDNR-LIB (CLONTECH ™) L3402 AN0086 amnion_normal puc18 L3403 AN0087 amnion_normal puc18 L3421 BT0634 breast puc18 L3432 CT0461 colon puc18 L3435 CT0465 colon puc18 L3450 CT0508 colon puc18 L3459 FT0175 prostate_tumor puc18 L3466 GN0020 placenta_normal puc18 L3480 GN0057 placenta_normal puc18 L3484 GN0067 placenta_normal puc18 L3485 GN0070 placenta_normal puc18 L3491 GN0076 placenta_normal puc18 L3496 HT0572 head_neck puc18 L3499 HT0617 head_neck puc18 L3503 HT0870 head_neck puc18 L3504 HT0873 head_neck puc18 L3506 HT0879 head_neck puc18 L3511 HT0900 head_neck puc18 L3516 HT0913 head_neck puc18 L3518 HT0915 head_neck puc18 L3521 HT0919 head_neck puc18 L3530 HT0939 head_neck puc18 L3561 TN0025 testis_normal puc18 L3562 TN0030 testis_normal puc18 L3603 UM0093 uterus puc18 L3618 UT0050 uterus_tumor puc18 L3632 UT0074 uterus_tumor puc18 L3642 ADA Adrenal gland pBLUESCRIPT ™ sk(−) L3643 ADB Adrenal gland pBLUESCRIPT ™ sk(−) L3644 ADC Adrenal gland pBLUESCRIPT ™ sk(−) L3645 Cu adrenal cortico adenoma for pBLUESCRIPT ™ Cushing''s syndrome sk(−) L3646 DCA pTriplEx2 L3649 DCB pTriplEx2 L3653 HTB Hypothalamus pBLUESCRIPT ™ sk(−) L3655 HTC Hypothalamus pBLUESCRIPT ™ sk(−) L3657 HTF Hypothalamus pBLUESCRIPT ™ sk(−) L3658 cdA pheochromocytoma pTriplEx2 L3659 CB cord blood pBLUESCRIPT ™ L3661 NPA pituitary pBLUESCRIPT ™ sk(−) L3665 NIH_MGC_75 kidney pDNR-LIB (CLONTECH ™) L3667 NIH_MGC_79 placenta pDNR-LIB (CLONTECH ™) L3673 AN0084 amnion_normal puc18 L3684 BT0812 breast puc18 L3705 CT0486 colon puc18 L3729 GN0079 placenta_normal puc18 L3744 HT0916 head_neck puc18 L3750 HT0945 head_neck puc18 L3783 TN0136 testis_normal puc18 L3807 UT0077 uterus_tumor puc18 L3808 UT0078 uterus_tumor puc18 L3811 NPC pituitary pBLUESCRIPT ™ sk(−) L3812 NPD pituitary pBLUESCRIPT ™ sk(−) L3813 TP pituitary tumor pTriplEx2 L3814 BM Bone marrow pTriplEx2 L3815 MDS Bone marrow pTriplEx2 L3816 HEMBA1 whole embryo, mainly head pME18SFL3 L3817 HEMBB1 whole embryo, mainly body pME18SFL3 L3819 NIH_MGC_76 liver pDNR-LIB (CLONTECH ™) L3824 NT2RM2 NT2 pME18SFL3 L3825 NT2RM4 NT2 pME18SFL3 L3826 NT2RP1 NT2 pUC19FL3 L3827 NT2RP2 NT2 pME18SFL3 L3828 NT2RP3 NT2 pME18SFL3 L3829 NT2RP4 NT2 pME18SFL3 L3831 OVARC1 ovary, tumor tissue pME18SFL3 L3832 PLACE1 placenta pME18SFL3 L3834 PLACE3 placenta pME18SFL3 L3837 THYRO1 thyroid gland pME18SFL3 L3841 NIH_MGC_18 large cell carcinoma lung pOTB7 L3871 NIH_MGC_19 neuroblastoma brain pOTB7 L3872 NCI_CGAP_Skn1 skin, normal, pCMV-SPORT6 4 pooled sa L3904 NCI_CGAP_Brn64 glioblastoma with EGFR brain pCMV-SPORT6 amplification L3905 NCI_CGAP_Brn67 anaplastic oligodendroglioma with brain pCMV-SPORT6 1p/19q loss L4497 NCI_CGAP_Br22 invasive ductal carcinoma, breast pCMV-SPORT6 3 pooled samples L4501 NCI_CGAP_Sub8 pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L4537 NCI_CGAP_Thy7 follicular adenoma (benign lesion) thyroid pAMP10 L4556 NCI_CGAP_HN13 squamous cell carcinoma tongue pCMV-SPORT6 L4558 NCI_CGAP_Pan3 pancreas pCMV-SPORT6 L4560 NCI_CGAP_Ut7 tumor uterus pCMV-SPORT6 L4669 NCI_CGAP_Ov41 serous papillary tumor ovary pCMV-SPORT6 L4747 NCI_CGAP_Brn41 oligodendroglioma brain pT7T3D-Pac (PHARMACIA ™) with a modified polylinker L5286 NCI_CGAP_Thy10 medullary carcinoma thyroid pAMP10 L5564 NCI_CGAP_HN20 normal pAMP1 head/neck tissue L5565 NCI_CGAP_Brn66 glioblastoma with probably TP53 brain pCMV-SPORT6 mutation and witho L5566 NCI_CGAP_Brn70 anaplastic oligodendroglioma brain pCMV- SPORT6.ccdb L5568 NCI_CGAP_HN21 nasopharyngeal carcinoma head/neck pAMP1 L5569 NCI_CGAP_HN17 normal epithelium nasopharynx pAMP10 L5574 NCI_CGAP_HN19 normal epithelium nasopharynx pAMP10 L5575 NCI_CGAP_Brn65 glioblastoma without EGFR brain pCMV-SPORT6 amplification L5622 NCI_CGAP_Skn3 skin pCMV-SPORT6 L5623 NCI_CGAP_Skn4 squamous cell carcinoma skin pCMV-SPORT6

Description of Table 5

Table 5 provides a key to the OMIM reference identification numbers disclosed in Table 1B.1, column 9. OMIM reference identification numbers (Column 1) were derived from Online Mendelian Inheritance in Man (Online Mendelian Inheritance in Man, OMIM. McKusick-Nathans Institute for Genetic Medicine, Johns Hopkins University (Baltimore, Md.) and National Center for Biotechnology Information, National Library of Medicine, (Bethesda, Md.) 2000. World Wide Web URL: http://www.ncbi.nlm.nih.gov/omim/). Column 2 provides diseases associated with the cytologic band disclosed in Table 1B.1, column 8, as determined using the Morbid Map database. TABLE 5 OMIM Refer- ence Description 100690 Myasthenic syndrome, slow-channel congenital, 601462 100710 Myasthenic syndrome, slow-channel congenital, 601462 101000 Meningioma, NF2-related, sporadic Schwannoma, sporadic 101000 Neurofibromatosis, type 2 101000 Neurolemmomatosis 101000 Malignant mesothelioma, sporadic 102578 Leukemia, acute promyelocytic, PML/RARA type 102770 Myoadenylate deaminase deficiency 103050 Autism, succinylpurinemic 103050 Adenylosuccinase deficiency 103850 Aldolase A deficiency 104770 Amyloidosis, secondary, susceptibility to 106100 Angioedema, hereditary 106150 Hypertension, essential, susceptibility to 106150 Preeclampsia, susceptibility to 106165 Hypertension, essential, 145500 106180 Myocardial infarction, susceptibility to 107300 Antithrombin III deficiency 107670 Apolipoprotein A-II deficiency 107741 Hyperlipoproteinemia, type III 107777 Diabetes insipidus, nephrogenic, autosomal recessive, 222000 108725 Atherosclerosis, susceptibility to 108985 Atrophia areata 109270 Renal tubular acidosis, distal, 179800 109270 Spherocytosis, hereditary 109270 [Acanthocytosis, one form] 109270 [Elliptocytosis, Malaysian-Melanesian type] 109270 Hemolytic anemia due to band 3 defect 109560 Leukemia/lymphoma, B-cell, 3 109690 Asthma, nocturnal, susceptibility to 109690 Obesity, susceptibility to 109700 Hemodialysis-related amyloidosis 110100 Blepharophimosis, epicanthus inversus, and ptosis, type 1 110700 Vivax malaria, susceptibility to 113100 Brachydactyly, type C 113900 Heart block, progressive familial, type I 114835 Monocyte carboxyesterase deficiency 115665 Cataract, congenital, Volkmann type 116800 Cataract, Marner type 116806 Colorectal cancer 116860 Cavernous angiomatous malformations 117700 [Hypoceruloplasminemia, hereditary] 117700 Hemosiderosis, systemic, due to aceruloplasminemia 118485 Polycystic ovary syndrome with hyperandrogenemia 118800 Choreoathetosis, familial paroxysmal 120070 Alport syndrome, autosomal recessive, 203780 120131 Alport syndrome, autosomal recessive, 203780 120131 Hematuria, familial benign 120140 Osteoarthrosis, precocious 120140 SED congenita 120140 SMED Strudwick type 120140 Stickler syndrome, type I 120140 Wagner syndrome, type II 120140 Achondrogenesis-hypochondrogenesis, type II 120140 Kniest dysplasia 120150 Osteogenesis imperfecta, 4 clinical forms, 166200, 166210, 259420, 166220 120150 Osteoporosis, idiopathic, 166710 120150 Ehlers-Danlos syndrome, type VIIA1, 130060 120215 Ehlers-Danlos syndrome, type I, 130000 120215 Ehlers-Danlos syndrome, type II, 130010 120260 Epiphyseal dysplasia, multiple, type 2, 600204 120435 Muir-Torre syndrome, 158320 120435 Colorectal cancer, hereditary, nonpolyposis, type 1 Ovarian cancer 120550 C1q deficiency, type A 120570 C1q deficiency, type B 120575 C1q deficiency, type C 120700 C3 deficiency 120950 C8 deficiency, type I 120960 C8 deficiency, type II 121050 Contractural arachnodactyly, congenital 121360 Myeloid leukemia, acute, M4Eo subtype 121800 Corneal dystrophy, crystalline, Schnyder 122720 Nicotine addiction, protection from 122720 Coumarin resistance, 122700 123000 Craniometaphyseal dysplasia 123270 [Creatine kinase, brain type, ectopic expression of] 123620 Cataract, cerulean, type 2, 601547 123660 Cataract, Coppock-like 123940 White sponge nevus, 193900 124030 Parkinsonism, susceptibility to 124030 Debrisoquine sensitivity 124200 Darier disease (keratosis follicularis) 125370 Dentatorubro-pallidoluysian atrophy 125660 Myopathy, desminopathic 125660 Cardiomyopathy 126090 Hyperphenylalaninemia due to pterin-4a-carbinolamine dehydratase deficiency, 264070 126337 Myxoid liposarcoma 126340 Xeroderma pigmentosum, group D, 278730 126391 DNA ligase I deficiency 126600 Drusen, radial, autosomal dominant 129010 Neuropathy, congenital hypomyelinating, 1 129900 EEC syndrome-1 130410 Glutaricaciduria, type IIB 130500 Elliptocytosis-1 131210 Atherosclerosis, susceptibility to 131244 Hirschsprung disease-2, 600155 131400 Eosinophilia, familial 132700 Cylindromatosis 133171 [Erythrocytosis, familial], 133100 133200 Erythrokeratodermia variabilis 133530 Xeroderma pigmentosum, group G, 278780 133701 Exostoses, multiple, type 2 133780 Vitreoretinopathy, exudative, familial 134790 Hyperferritinemia-cataract syndrome, 600886 135300 Fibromatosis, gingival 135940 Ichthyosis vulgaris, 146700 136132 [Fish-odor syndrome], 602079 136350 Pfeiffer syndrome, 101600 136435 Ovarian dysgenesis, hypergonadotropic, with normal karyotype, 233300 136550 Macular dystrophy, North Carolina type 136836 Fucosyltransferase-6 deficiency 138030 [Hyperproglucagonemia] 138040 Cortisol resistance 138140 Glucose transport defect, blood-brain barrier 138160 Diabetes mellitus, noninsulin-dependent 138160 Fanconi-Bickel syndrome, 227810 138300 Hemolytic anemia due to glutathione reductase deficiency 138570 Non-insulin dependent diabetes mellitus, susceptibility to 138700 [Apolipoprotein H deficiency] 138981 Pulmonary alveolar proteinosis, 265120 139250 Isolated growth hormone deficiency, Illig type with absent GH and Kowarski type with bioinactive GH 139350 Epidermolytic hyperkeratosis, 113800 139350 Keratoderma, palmoplantar, nonepidermolytic 140100 [Anhaptoglobinemia] 140100 [Hypohaptogloginemia] 141750 Alpha-thalassemia/mental retardation syndrome, type 1 141800 Methemoglobinemias, alpha- 141800 Thalassemias, alpha- 141800 Erythremias, alpha- 141800 Heinz body anemias, alpha- 141850 Thalassemia, alpha- 141850 Erythrocytosis 141850 Heinz body anemia 141850 Hemoglobin H disease 141850 Hypochromic microcytic anemia 142335 Hereditary persistence of fetal hemoglobin, heterocellular, Indian type 142600 Hemolytic anemia due to hexokinase deficiency 142989 Synpolydactyly, type II, 186000 143890 Hypercholesterolemia, familial 145001 Hyperparathyroidism-jaw tumor syndrome 145260 Pseudohypoaldosteronism, type II 145505 Hypertension, essential 145981 Hypocalciuric hypercalcemia, type II 146200 Hypoparathyroidism, familial 146760 [IgG receptor I, phagocytic, familial deficiency of] 146790 Lupus nephritis, susceptibility to 147141 Leukemia, acute lymphoblastic 147440 Growth retardation with deafness and mental retardation 147670 Rabson-Mendenhall syndrome 147670 Diabetes mellitus, insulin-resistant, with acanthosis nigricans 147670 Leprechaunism 147781 Atopy, susceptibility to 148040 Epidermolysis bullosa simplex, Koebner, Dowling-Meara, and Weber-Cockayne types, 131900, 131760, 131800 148041 Pachyonychia congenita, Jadassohn-Lewandowsky type, 167200 148043 Meesmann corneal dystrophy, 122100 148065 White sponge nevus, 193900 148070 Liver disease, susceptibility to, from hepatotoxins or viruses 148080 Epidermolytic hyperkeratosis, 113800 148370 Keratolytic winter erythema 148900 Klippel-Feil syndrome with laryngeal malformation 150200 [Placental lactogen deficiency] 150210 Lactoferrin-deficient neutrophils, 245480 150292 Epidermolysis bullosa, Herlitz junctional type, 226700 151440 Leukemia, T-cell acute lymphoblastoid 151670 Hepatic lipase deficiency 152427 Long QT syndrome-2 152445 Vohwinkel syndrome, 124500 152445 Erythrokeratoderma, progressive symmetric, 602036 152760 Hypogonadotropic hypogonadism due to GNRH deficiency, 227200 152780 Hypogonadism, hypergonadotropic 152780 Male pseudohermaphroditism due to defective LH 152790 Precocious puberty, male, 176410 152790 Leydig cell hypoplasia 153454 Ehlers-Danlos syndrome, type VI, 225400 153455 Cutis laxa, recessive, type I, 219100 154275 Malignant hyperthermia susceptibility 2 154276 Malignant hyperthermia susceptibility 3 154545 Chronic infections, due to opsonin defect 154550 Carbohydrate-deficient glycoprotein syndrome, type Ib, 602579 155555 [Red hair/fair skin] 155555 UV-induced skin damage, vulnerability to 156232 Mesomelic dysplasia, Kantaputra type 156850 Cataract, congenital, with microphthalmia 157147 Abetalipoproteinemia, 200100 157170 Holoprosencephaly-2 157640 PEO with mitochondrial DNA deletions, type 1 158590 Spinal muscular atrophy-4 159000 Muscular dystrophy, limb-girdle, type 1A 159001 Muscular dystrophy, limb-girdle, type 1B 160760 Cardiomyopathy, familial hypertrophic, 1, 192600 160760 Central core disease, one form 160781 Cardiomyopathy, hypertrophic, mid-left ventricular chamber type 160900 Myotonic dystrophy 162150 Obestiy with impaired prohormone processing, 600955 162200 Neurofibromatosis, type 1 162200 Watson syndrome, 193520 162400 Neuropathy, hereditary sensory and autonomic, type 1 163729 Hypertension, pregnancy-induced 163950 Noonan syndrome-1 163950 Cardiofaciocutaneous syndrome, 115150 164731 Ovarian carcinoma, 167000 164770 Myeloid malignancy, predisposition to 164953 Liposarcoma 167410 Rhabdomyosarcoma, alveolar, 268220 168360 Paraneoplastic sensory neuropathy 168450 Hypoparathyroidism, autosomal dominant 168450 Hypoparathyroidism, autosomal recessive 168468 Metaphyseal chondrodysplasia, Murk Jansen type, 156400 168500 Parietal foramina 169600 Hailey-Hailey disease 170500 Myotonia congenita, atypical acetazolamide-responsive 170500 Paramyotonia congenita, 168300 170500 Hyperkalemic periodic paralysis 171190 Hypertension, essential, 145500 171650 Lysosomal acid phosphatase deficiency 171760 Hypophosphatasia, adult, 146300 171760 Hypophosphatasia, infantile, 241500 172400 Hemolytic anemia due to glucosephosphate isomerase deficiency 172400 Hydrops fetalis, one form 172430 Enolase deficiency 172471 Glycogenosis, hepatic, autosomal 172490 Phosphorylase kinase deficiency of liver and muscle, 261750 173470 Glanzmann thrombasthenia, type B 173610 Platelet alpha/delta storage pool deficiency 173850 Polio, susceptibility to 173870 Xeroderma pigmentosum 173870 Fanconi anemia 173910 Polycystic kidney disease, adult, type II 174000 Medullary cystic kidney disease, AD 174900 Polyposis, juvenile intestinal 176100 Porphyria cutanea tarda 176100 Porphyria, hepatoerythropoietic 176450 Sacral agenesis-1 176830 Obesity, adrenal insufficiency, and red hair 176830 ACTH deficiency 176930 Dysprothrombinemia 176930 Hypoprothrombinemia 176960 Pituitary tumor, invasive 177400 Apnea, postanesthetic 178300 Ptosis, hereditary congenital, 1 178600 Pulmonary hypertension, familial primary 178640 Pulmonary alveolar proteinosis, congenital, 265120 179095 Male infertility 179755 Renal cell carcinoma, papillary, 1 180069 Retinal dystrophy, autosomal recessive, childhood-onset 180069 Retinitis pigmentosa-20 180069 Leber congenital amaurosis-2, 204100 180071 Retinitis pigmentosa, autosomal recessive 180100 Retinitis pigmentosa-1 180105 Retinitis pigmentosa-10 180380 Night blindness, congenital stationery, rhodopsin-related 180380 Retinitis pigmentosa, autosomal recessive 180380 Retinitis pigmentosa-4, autosomal dominant 180901 Malignant hyperthermia susceptibility 1, 145600 180901 Central core disease, 117000 181405 Scapuloperoneal spinal muscular atrophy, New England type 181430 Scapuloperoneal syndrome, myopathic type 181460 Schistosoma mansoni, susceptibility/resistance to 182138 Anxiety-related personality traits 182280 Small-cell cancer of lung 182290 Smith-Magenis syndrome 182380 Glucose/galactose malabsorption 182381 Renal glucosuria, 253100 182600 Spastic paraplegia-3A 182601 Spastic paraplegia-4 182860 Pyropoikilocytosis 182860 Spherocytosis, recessive 182860 Elliptocytosis-2 182900 Spherocytosis-2 185800 Symphalangism, proximal 186580 Arthrocutaneouveal granulomatosis 186880 Leukemia/lymphoma, T-cell 186921 Leukemia, T-cell acute lymphoblastic 187040 Leukemia-1, T-cell acute lymphoblastic 188070 Bleeding disorder due to defective thromboxane A2 receptor 188450 Goiter, adolescent multinodular 188450 Goiter, nonendemic, simple 188450 Hypothyroidism, hereditary congenital 188826 Sorsby fundus dystrophy, 136900 189800 Preeclampsia/eclampsia 190040 Meningioma, SIS-related 190040 Dermatofibrosarcoma protuberans 190040 Giant-cell fibroblastoma 190195 Ichthyosiform erythroderma, congenital, 242100 190195 Ichthyosis, lamellar, autosomal recessive, 242300 190198 Leukemia, T-cell acute lymphoblastic 190300 Tremor, familial essential, 1 190605 Triphalangeal thumb-polysyndactyly syndrome 191044 Cardiomyopathy, familial hypertrophic 191092 Tuberous sclerosis-2 191315 Insensitivity to pain, congenital, with anhidrosis, 256800 192090 Ovarian carcinoma 192090 Breast cancer, lobular 192090 Endometrial carcinoma 192090 Gastric cancer, familial, 137215 192340 Diabetes insipidus, neurohypophyseal, 125700 192974 Neonatal alloimmune thrombocytopenia 192974 Glycoprotein Ia deficiency 193300 Renal cell carcinoma 193300 von Hippel-Lindau syndrome 193500 Rhabdomyosarcoma, alveolar, 268220 193500 Waardenburg syndrome, type I 193500 Waardenburg syndrome, type III, 148820 193500 Craniofacial-deafness-hand syndrome, 122880 201450 Acyl-CoA dehydrogenase, medium chain, deficiency of 201460 Acyl-CoA dehydrogenase, long chain, deficiency of 201475 VLCAD deficiency 201810 3-beta-hydroxysteroid dehydrogenase, type II, deficiency 203300 Hermansky-Pudlak syndrome 203500 Alkaptonuria 205100 Amyotrophic lateral sclerosis, juvenile 205900 Anemia, Diamond-Blackfan 207750 Hyperlipoproteinemia, type Ib 208250 Jacobs syndrome 208400 Aspartylglucosaminuria 212138 Carnitine-acylcarnitine translocase deficiency 216550 Cohen syndrome 216900 Achromatopsia 217300 Cornea plana congenita, recessive 217800 Macular corneal dystrophy 218030 Apparent mineralocorticoid excess, hypertension due to 221770 Polycystic lipomembranous osteodysplasia with sclerosing leukencephalopathy 221820 Gliosis, familial progressive subcortical 222700 Lysinuric protein intolerance 222745 DECR deficiency 222800 Hemolytic anemia due to bisphosphoglycerate mutase deficiency 222900 Sucrose intolerance 225500 Ellis-van Creveld syndrome 227645 Fanconi anemia, type C 227646 Fanconi anemia, type D 227650 Fanconi anemia, type A 229700 Fructose-bisphosphatase deficiency 229800 [Fructosuria] 230000 Fucosidosis 230400 Galactosemia 230800 Gaucher disease 230800 Gaucher disease with cardiovascular calcification 231550 Achalasia-addisonianism-alacrimia syndrome 231670 Glutaricaciduria, type I 231675 Glutaricaciduria, type IIC 231680 Glutaricaciduria, type IIA 232300 Glycogen storage disease II 232700 Glycogen storage disease VI 232800 Glycogen storage disease VII 233700 Chronic granulomatous disease due to deficiency of NCF-1 234200 Neurodegeneration with brain iron accumulation 236250 Homocystinuria due to MTHFR deficiency 236730 Urofacial syndrome 237300 Carbamoylphosphate synthetase I deficiency 239100 Van Buchem disease 240400 Scurvy 245200 Krabbe disease 245900 Norum disease 245900 Fish-eye disease 246450 HMG-CoA lyase deficiency 248510 Mannosidosis, beta- 248600 Maple syrup urine disease, type Ia 248610 Maple syrup urine disease, type II 249000 Meckel syndrome 250250 Cartilage-hair hypoplasia 250790 Methemoglobinemia due to cytochrome b5 deficiency 250850 Hypermethioninemia, persistent, autosomal dominant, due to methionine adenosyltransferase I/III deficiency 251170 Mevalonicaciduria 251600 Microphthalmia, autosomal recessive 252500 Mucolipidosis II 252500 Mucolipidosis III 252900 Sanfilippo syndrome, type A 253000 Mucopolysaccharidosis IVA 253250 Mulibrey nanism 255800 Schwartz-Jampel syndrome 256030 Nemaline myopathy-2 256540 Galactosialidosis 256700 Neuroblastoma 256731 Ceroid-lipofuscinosis, neuronal-5, variant late infantile 257200 Niemann-Pick disease, type A 257200 Niemann-Pick disease, type B 258501 3-methylglutaconicaciduria, type III 258900 Oroticaciduria 259900 Hyperoxaluria, primary, type 1 262000 Bjornstad syndrome 266200 Anemia, hemolytic, due to PK deficiency 270100 Situs inversus viscerum 270200 Sjogren-Larsson syndrome 272750 GM2-gangliosidosis, AB variant 272800 Tay-Sachs disease 272800 [Hex A pseudodeficiency] 272800 GM2-gangliosidosis, juvenile, adult 273800 Thrombocytopenia, neonatal alloimmune 273800 Glanzmann thrombasthenia, type A 276600 Tyrosinemia, type II 276700 Tyrosinemia, type I 276710 Tyrosinemia, type III 276900 Usher syndrome, type 1A 276901 Usher syndrome, type 2 276902 Usher syndrome, type 3 277700 Werner syndrome 278700 Xeroderma pigmentosum, group A 278760 Xeroderma pigmentosum, group F 300000 Opitz G syndrome, type I 300008 Nephrolithiasis, type I, 310468 300008 Proteinuria, low molecular weight, with hypercalciuric nephrocalcinosis 300008 Dent disease, 300009 300008 Hypophosphatemia, type III 300011 Menkes disease, 309400 300011 Occipital horn syndrome, 304150 300011 Cutis laxa, neonatal 300031 Mental retardation, X-linked, FRAXF type 300044 Wernicke-Korsakoff syndrome, susceptibility to 300046 Mental retardation, X-linked 23, nonspecific 300047 Mental retardation, X-linked 20 300048 Intestinal pseudoobstruction, neuronal, X-linked 300049 Nodular heterotopia, bilateral periventricular 300049 BPNH/MR syndrome 300055 Mental retardation with psychosis, pyramidal signs, and macroorchidism 300066 Deafness, X-linked 6, sensorineural 300071 Night blindness, congenital stationary, type 2 300075 Coffin-Lowry syndrome, 303600 300077 Mental retardation, X-linked 29 300100 Adrenoleukodystrophy 300100 Adrenomyeloneuropathy 300104 Mental retardation, X-linked nonspecific, 309541 300110 Night blindness, congenital stationary, X-linked incomplete, 300071 300123 Mental retardation with isolated growth hormone deficiency 300126 Dyskeratosis congenita-1, 305000 300127 Mental retardation, X-linked, 60 300310 Agammaglobulinemia, type 2, X-linked 300600 Ocular albinism, Forsius-Eriksson type 301000 Thrombocytopenia, X-linked, 313900 301000 Wiskott-Aldrich syndrome 301200 Amelogenesis imperfecta 301201 Amelogenesis imperfecta-3, hypoplastic type 301220 Partington syndrome II 301590 Anophthalmos-1 301830 Arthrogryposis, X-linked (spinal muscular atrophy, infantile, X- linked) 301835 Arts syndrome 301845 Bazex syndrome 302060 Noncompaction of left ventricular myocardium, isolated 302060 Barth syndrome 302060 Cardiomyopathy, X-linked dilated, 300069 302060 Endocardial fibroelastosis-2 302350 Nance-Horan syndrome 302801 Charcot-Marie-Tooth neuropathy, X-linked-2, recessive 302960 Chondrodysplasia punctata, X-linked dominant 303700 Colorblindness, blue monochromatic 303800 Colorblindness, deutan 303900 Colorblindness, protan 304040 Charcot-Marie-Tooth neuropathy, X-linked-1, dominant, 302800 304050 Aicardi syndrome 304110 Craniofrontonasal dysplasia 304800 Diabetes insipidus, nephrogenic 305100 Anhidrotic ectodermal dysplasia 305435 Heterocellular hereditary persistence of fetal hemoglobin, Swiss type 305450 FG syndrome 305900 Favism 305900 G6PD deficiency 305900 Hemolytic anemia due to G6PD deficiency 306000 Glycogenosis, X-linked hepatic, type I 306000 Glycogenosis, X-linked hepatic, type II 306100 Gonadal dysgenesis, XY female type 306700 Hemophilia A 306995 [Homosexuality, male] 307150 Hypertrichosis, congenital generalized 307800 Hypophosphatemia, hereditary 308310 Incontinentia pigmenti, familial 308800 Keratosis follicularis spinulosa decalvans 308840 Spastic paraplegia, 312900 308840 Hydrocephalus due to aqueductal stenosis, 307000 308840 MASA syndrome, 303350 309200 Manic-depressive illness, X-linked 309470 Mental retardation, X-linked, syndromic-3, with spastic diplegia 309500 Renpenning syndrome-1 309510 Mental retardation, X-linked, syndromic-1, with dystonic movements, ataxia, and seizures 309530 Mental retardation, X-linked 1, non-dysmorphic 309548 Mental retardation, X-linked, FRAXE type 309585 Mental retardation, X-linked, syndromic-6, with gynecomastia and obesity 309605 Mental retardation, X-linked, syndromic-4, with congenital contractures and low fingertip arches 309610 Mental retardation, X-linked, syndromic-2, with dysmorphism and cerebral atrophy 309620 Mental retardation-skeletal dysplasia 309850 Brunner syndrome 309900 Mucopolysaccharidosis II 310300 Emery-Dreifuss muscular dystrophy 310400 Myotubular myopathy, X-linked 310460 Myopia-1 310460 Bornholm eye disease 310490 Cowchock syndrome 311050 Optic atrophy, X-linked 311200 Oral-facial-digital syndrome 1 311300 Otopalatodigital syndrome, type I 311510 Waisman parkinsonism-mental retardation syndrome 311850 Phosphoribosyl pyrophosphate synthetase-related gout 312040 N syndrome, 310465 312060 Properdin deficiency, X-linked 312170 Pyruvate dehydrogenase deficiency 312700 Retinoschisis 312760 Turner syndrome 313400 Spondyloepiphyseal dysplasia tarda 313700 Perineal hypospadias 313700 Prostate cancer 313700 Spinal and bulbar muscular atrophy of Kennedy, 313200 313700 Breast cancer, male, with Reifenstein syndrome 313700 Androgen insensitivity, several forms 314250 Dystonia-3, torsion, with parkinsonism, Filipino type 314300 Goeminne TKCR syndrome 314400 Cardiac valvular dysplasia-1 314580 Wieacker-Wolff syndrome 600040 Colorectal cancer 600079 Colon cancer 600101 Deafness, autosomal dominant 2 600119 Muscular dystrophy, Duchenne-like, type 2 600119 Adhalinopathy, primary 600138 Retinitis pigmentosa-11 600140 Rubenstein-Taybi syndrome, 180849 600163 Long QT syndrome-3 600173 SCID, autosomal recessive, T-negative/B-positive type 600175 Spinal muscular atrophy, congenital nonprogressive, of lower limbs 600194 Ichthyosis bullosa of Siemens, 146800 600223 Spinocerebellar ataxia-4 600231 Palmoplantar keratoderma, Bothnia type 600234 HMG-CoA synthease-2 deficiency 600243 Temperature-sensitive apoptosis 600258 Colorectal cancer, hereditary nonpolyposis, type 3 600266 Resistance/susceptibility to TB, etc. 600273 Polycystic kidney disease, infantile severe, with tuberous sclerosis 600276 Cerebral arteriopathy with subcortical infarcts and leukoencephalopathy, 125310 600281 Non-insulin-dependent diabetes mellitus, 125853 600281 MODY, type 1, 125850 600309 Atrioventricular canal defect-1 600310 Pseudoachondroplasia, 177170 600310 Epiphyseal dysplasia, multiple 1, 132400 600320 Insulin-dependent diabetes mellitus-5 600332 Rippling muscle disease-1 600359 Bartter syndrome, type 2 600374 Bardet-Biedl syndrome 4 600510 Pigment dispersion syndrome 600512 Epilepsy, partial 600525 Trichodontoosseous syndrome, 190320 600536 Myopathy, congenital 600593 Craniosynostosis, Adelaide type 600617 Lipoid adrenal hyperplasia, 201710 600623 Prostate cancer, 176807 600631 Enuresis, nocturnal, 1 600650 Myopathy due to CPT II deficiency, 255110 600650 CPT deficiency, hepatic, type II, 600649 600652 Deafness, autosomal dominant 4 600698 Salivary adenoma 600698 Uterine leiomyoma 600698 Lipoma 600698 Lipomatosis, mutiple, 151900 600722 Ceroid lipofuscinosis, neuronal, variant juvenile type, with granular osmiophilic deposits 600722 Ceroid lipofuscinosis, neuronal-1, infantile, 256730 600725 Holoprosencephaly-3, 142945 600757 Orofacial cleft-3 600759 Alzheimer disease-4 600792 Deafness, autosomal recessive 5 600807 Bronchial asthma 600808 Enuresis, nocturnal, 2 600811 Xeroderma pigmentosum, group E, DDB-negative subtype, 278740 600850 Schizophrenia disorder-4 600852 Retinitis pigmentosa-17 600881 Cataract, congenital, zonular, with sutural opacities 600882 Charcot-Marie-Tooth neuropathy-2B 600897 Cataract, zonular pulverulent-1, 116200 600918 Cystinuria, type III 600956 Persistent Mullerian duct syndrome, type II, 261550 600957 Persistent Mullerian duct syndrome, type I, 261550 600958 Cardiomyopathy, familial hypertrophic, 4, 115197 600968 Gitelman syndrome, 263800 600975 Glaucoma 3, primary infantile, B 600995 Nephrotic syndrome, idiopathic, steroid-resistant 600996 Arrhythmogenic right ventricular dysplasia-2 601097 Neuropathy, recurrent, with pressure palsies, 162500 601097 Charcot-Marie-Tooth neuropathy-1A, 118220 601097 Dejerine-Sottas disease, PMP22 related, 145900 601105 Pycnodysostosis, 265800 601199 Neonatal hyperparathyroidism, 239200 601199 Hypocalcemia, autosomal dominant, 601198 601199 Hypocalciuric hypercalcemia, type I, 145980 601238 Cerebellar ataxia, Cayman type 601277 Ichthyosis, lamellar, type 2 601284 Hereditary hemorrhagic telangiectasia-2, 600376 601295 Bile acid malabsorption, primary 601309 Basal cell carcinoma, sporadic 601309 Basal cell nevus syndrome, 109400 601313 Polycystic kidney disease, adult type I, 173900 601369 Deafness, autosomal dominant 9 601386 Deafness, autosomal recessive 12 601402 Leukemia, myeloid, acute 601412 Deafness, autosomal dominant 7 601414 Retinitis pigmentosa-18 601458 Inflammatory bowel disease-2 601493 Cardiomyopathy, dilated 1C 601517 Spinocerebellar ataxia-2, 183090 601518 Prostate cancer, hereditary, 1, 176807 601596 Charcot-Marie-Tooth neuropathy, demyelinating 601604 Mycobacterial and salmonella infections, susceptibility to 601650 Paraganglioma, familial nonchromaffin, 2 601652 Glaucoma 1A, primary open angle, juvenile-onset, 137750 601669 Hirschsprung disease, one form 601676 Acute insulin response 601682 Glaucoma 1C, primary open angle 601691 Retinitis pigmentosa-19, 601718 601691 Stargardt disease-1, 248200 601691 Cone-rod dystrophy 3 601691 Fundus flavimaculatus with macular dystrophy, 248200 601692 Reis-Bucklers corneal dystrophy 601692 Corneal dystrophy, Avellino type 601692 Corneal dystrophy, Groenouw type I, 121900 601692 Corneal dystrophy, lattice type I, 122200 601718 Retinitis pigmentosa-19 601744 Systemic lupus erythematosus, susceptibility to, 1 601769 Osteoporosis, involutional 601769 Rickets, vitamin D-resistant, 277440 601771 Glaucoma 3A, primary infantile, 231300 601780 Ceroid-lipofuscinosis, neuronal-6, variant late infantile 601785 Carbohydrate-deficient glycoprotein syndrome, type I, 212065 601843 Hypothyroidism, congenital, 274400 601844 Pseudohypoaldosteronism type II 601846 Muscular dystrophy with rimmed vacuoles 601863 Bare lymphocyte syndrome, complementation group C 601928 Monilethrix, 158000 601954 Muscular dystrophy, limb-girdle, type 2G 601975 Ectodermal dysplasia/skin fragility syndrome 602025 Obesity/hyperinsulinism, susceptibility to 602078 Fibrosis of extraocular muscles, congenital, 2 602085 Postaxial polydactyly, type A2 602086 Arrhythmogenic right ventricular dysplasia-3 602088 Nephronophthisis, infantile 602089 Hemangioma, capillary, hereditary 602092 Deafness, autosomal recessive 18 602094 Lipodystrophy, familial partial 602116 Glioma 602121 Deafness, autosomal dominant nonsyndromic sensorineural, 1, 124900 602134 Tremor, familial essential, 2 602136 Refsum disease, infantile, 266510 602136 Zellweger syndrome-1, 214100 602136 Adrenoleukodystrophy, neonatal, 202370 602153 Monilethrix, 158000 602216 Peutz-Jeghers syndrome, 175200 602225 Cone-rod retinal dystrophy-2, 120970 602225 Leber congenital amaurosis, type III 602279 Oculopharyngeal muscular dystorphy, 164300 602279 Oculopharyngeal muscular dystrophy, autosomal recessive, 257950 602363 Ellis-van Creveld-like syndrome 602403 Alzheimer disease, susceptibility to 602447 Coronary artery disease, susceptibility to 602460 Deafness, autosomal dominant 15, 602459 602477 Febrile convulsions, familial, 2 602491 Hyperlipidemia, familial combined, 1 602522 Bartter syndrome, infantile, with sensorineural deafness 602568 Homocystinuria-megaloblastic anemia, cb1 E type, 236270 602574 Deafness, autosomal dominant 12, 601842 602574 Deafness, autosomal dominant 8, 601543 602629 Dystonia-6, torsion 602666 Deafness, autosomal recessive 3, 600316 602716 Nephrosis-1, congenital, Finnish type, 256300 602772 Retinitis pitmentosa-24 602782 Faisalabad histiocytosis 602783 Spastic paraplegia-7

Mature Polypeptides

The present invention also encompasses mature forms of a polypeptide having the amino acid sequence of SEQ ID NO:Y and/or the amino acid sequence encoded by the cDNA in a deposited clone. Polynucleotides encoding the mature forms (such as, for example, the polynucleotide sequence in SEQ ID NO:X and/or the polynucleotide sequence contained in the cDNA of a deposited clone) are also encompassed by the invention. Moreover, fragments or variants of these polypeptides (such as, fragments as described herein, polypeptides at least 80%, 85%, 90%, 95%, 96%, 97%, 98%, 99%, or 100% identical to these polypeptides, or polypeptides encoded by a polynucleotide that hybridizes under stringent conditions to the complementary strand of the polynucleotide encoding these polypeptides) are also encompassed by the invention. In preferred embodiments, these fragments or variants retain one or more functional activities of the full-length or mature form of the polypeptide (e.g., biological activity (such as, for example, activity useful in detecting, preventing, diagnosing, prognosticating, treating, and/or ameliorating cancer and other hyperproliferative disorders), antigenicity (ability to bind, or compete with a polypeptide of the invention for binding, to an anti-polypeptide of the invention antibody), immunogenicity (ability to generate antibody which binds to a specific polypeptide of the invention), ability to form multimers with polypeptides of the invention, and ability to bind to a receptor or ligand for a polypeptide of the invention). Antibodies that bind the polypeptides of the invention, and polynucleotides encoding these polypeptides are also encompassed by the invention.

According to the signal hypothesis, proteins secreted by mammalian cells have a signal or secretary leader sequence which is cleaved from the mature protein once export of the growing protein chain across the rough endoplasmic reticulum has been initiated. Most mammalian cells and even insect cells cleave secreted proteins with the same specificity. However, in some cases, cleavage of a secreted protein is not entirely uniform, which results in two or more mature species of the protein. Further, it has long been known that cleavage specificity of a secreted protein is ultimately determined by the primary structure of the complete protein, that is, it is inherent in the amino acid sequence of the polypeptide.

Methods for predicting whether a protein has a signal sequence, as well as the cleavage point for that sequence, are available. For instance, the method of McGeoch, Virus Res. 3:271-286 (1985), uses the information from a short N-terminal charged region and a subsequent uncharged region of the complete (uncleaved) protein. The method of von Heinje, Nucleic Acids Res. 14:4683-4690 (1986) uses the information from the residues surrounding the cleavage site, typically residues −13 to +2, where +1 indicates the amino terminus of the secreted protein. The accuracy of predicting the cleavage points of known mammalian secretory proteins for each of these methods is in the range of 75-80%. (von Heinje, supra.) However, the two methods do not always produce the same predicted cleavage point(s) for a given protein.

In the present case, the deduced amino acid sequence of the secreted polypeptide was analyzed by a computer program called SignalP (Henrik Nielsen et al., Protein Engineering 10:1-6 (1997)), which predicts the cellular location of a protein based on the amino acid sequence. As part of this computational prediction of localization, the methods of McGeoch and von Heinje are incorporated. The analysis of the amino acid sequences of the secreted proteins described herein by this program provided the results shown in Table 1A.

In specific embodiments, polypeptides of the invention comprise, or alternatively consist of, the predicted mature form of the polypeptide as delineated in columns 14 and 15 of Table 1A. Moreover, fragments or variants of these polypeptides (such as, fragments as described herein, polypeptides at least 80%, 85%, 90%, 95%, 96%, 97%, 98%, 99%, or 100% identical to these polypeptides, or polypeptides encoded by a polynucleotide that hybridizes under stringent conditions to the complementary strand of the polynucleotide encoding these polypeptides) are also encompassed by the invention. In preferred embodiments, these fragments or variants retain one or more functional activities of the full-length or mature form of the polypeptide (e.g., biological activity (such as, for example, activity useful in detecting, preventing, diagnosing, prognosticating, treating, and/or ameliorating cancer and other hyperproliferative disorders), antigenicity (ability to bind, or compete with a polypeptide of the invention for binding, to an anti-polypeptide of the invention antibody), immunogenicity (ability to generate antibody which binds to a specific polypeptide of the invention), ability to form multimers with polypeptides of the invention, and ability to bind to a receptor or ligand for a polypeptide of the invention). Antibodies that bind the polypeptides of the invention, and polynucleotides encoding these polypeptides are also encompassed by the invention.

Polynucleotides encoding proteins comprising, or consisting of, the predicted mature form of polypeptides of the invention (e.g., polynucleotides having the sequence of SEQ ID NO: X (Table 1A, column 4), the sequence delineated in columns 7 and 8 of Table 1A, and a sequence encoding the mature polypeptide delineated in columns 14 and 15 of Table 1A (e.g., the sequence of SEQ ID NO:X encoding the mature polypeptide delineated in columns 14 and 15 of Table 1)) are also encompassed by the invention, as are fragments or variants of these polynucleotides (such as, fragments as described herein, polynucleotides at least 80%, 85%, 90%, 95%, 96%, 97%, 98%, 99%, or 100% identical to these polynucleotides, and nucleic acids which hybridizes under stringent conditions to the complementary strand of the polynucleotide).

As one of ordinary skill would appreciate, however, cleavage sites sometimes vary from organism to organism and cannot be predicted with absolute certainty. Accordingly, the present invention provides secreted polypeptides having a sequence shown in SEQ ID NO:Y which have an N-terminus beginning within 15 residues of the predicted cleavage point (i.e., having 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, or 15 more or less contiguous residues of SEQ ID NO:Y at the N-terminus when compared to the predicted mature form of the polypeptide (e.g., the mature polypeptide delineated in columns 14 and 15 of Table 1). Similarly, it is also recognized that in some cases, cleavage of the signal sequence from a secreted protein is not entirely uniform, resulting in more than one secreted species. These polypeptides, and the polynucleotides encoding such polypeptides, are contemplated by the present invention.

Moreover, the signal sequence identified by the above analysis may not necessarily predict the naturally occurring signal sequence. For example, the naturally occurring signal sequence may be further upstream from the predicted signal sequence. However, it is likely that the predicted signal sequence will be capable of directing the secreted protein to the ER. Nonetheless, the present invention provides the mature protein produced by expression of the polynucleotide sequence of SEQ ID NO:X and/or the polynucleotide sequence contained in the cDNA of a deposited clone, in a mammalian cell (e.g., COS cells, as described below). These polypeptides, and the polynucleotides encoding such polypeptides, are contemplated by the present invention.

Polynucleotide and Polypeptide Variants

The present invention is also directed to variants of the polynucleotide sequence disclosed in SEQ ID NO:X or the complementary strand thereto, nucleotide sequences encoding the polypeptide of SEQ ID NO:Y, the nucleotide sequence of SEQ ID NO:X that encodes the polypeptide sequence as defined in columns 13 and 14 of Table 1A, nucleotide sequences encoding the polypeptide sequence as defined in columns 13 and 14 of Table 1A, the nucleotide sequence of SEQ ID NO:X encoding the polypeptide sequence as defined in Table 1B, the nucleotide sequence as defined in columns 8 and 9 of Table 2, nucleotide sequences encoding the polypeptide encoded by the nucleotide sequence as defined in columns 8 and 9 of Table 2, the nucleotide sequence as defined in column 6 of Table 1C, nucleotide sequences encoding the polypeptide encoded by the nucleotide sequence as defined in column 6 of Table 1C, the cDNA sequence contained in ATCC™ Deposit No:Z, nucleotide sequences encoding the polypeptide encoded by the cDNA sequence contained in ATCC™ Deposit No:Z, and/or nucleotide sequences encoding a mature (secreted) polypeptide encoded by the cDNA sequence contained in ATCC™ Deposit No:Z.

The present invention also encompasses variants of the polypeptide sequence disclosed in SEQ ID NO:Y, the polypeptide as defined in columns 13 and 14 of Table 1A, the polypeptide sequence as defined in columns 6 and 7 of Table 1B.1, a polypeptide sequence encoded by the polynucleotide sequence in SEQ ID NO:X, a polypeptide sequence encoded by the nucleotide sequence as defined in columns 8 and 9 of Table 2, a polypeptide sequence encoded by the nucleotide sequence as defined in column 6 of Table 1C, a polypeptide sequence encoded by the complement of the polynucleotide sequence in SEQ ID NO:X, the polypeptide sequence encoded by the cDNA sequence contained in ATCC™ Deposit No:Z and/or a mature (secreted) polypeptide encoded by the cDNA sequence contained in ATCC™ Deposit No:Z.

“Variant” refers to a polynucleotide or polypeptide differing from the polynucleotide or polypeptide of the present invention, but retaining essential properties thereof. Generally, variants are overall closely similar, and, in many regions, identical to the polynucleotide or polypeptide of the present invention.

Thus, one aspect of the invention provides an isolated nucleic acid molecule comprising, or alternatively consisting of, a polynucleotide having a nucleotide sequence selected from the group consisting of: (a) a nucleotide sequence described in SEQ ID NO:X or contained in the cDNA sequence of ATCC™ Deposit No:Z; (b) a nucleotide sequence in SEQ ID NO:X or the cDNA in ATCC™ Deposit No:Z which encodes the complete amino acid sequence of SEQ ID NO:Y or the complete amino acid sequence encoded by the cDNA in ATCC™ Deposit No:Z; (c) a nucleotide sequence in SEQ ID NO:X or the cDNA in ATCC™ Deposit No:Z which encodes a mature polypeptide (i.e., a secreted polypeptide (e.g., as delineated in columns 14 and 15 of Table 1A)); (d) a nucleotide sequence in SEQ ID NO:X or the cDNA sequence of ATCC™ Deposit No:Z, which encodes a biologically active fragment of a polypeptide; (e) a nucleotide sequence in SEQ ID NO:X or the cDNA sequence of ATCC™ Deposit No:Z, which encodes an antigenic fragment of a polypeptide; (f) a nucleotide sequence encoding a polypeptide comprising the complete amino acid sequence of SEQ ID NO:Y or the complete amino acid sequence encoded by the cDNA in ATCC™ Deposit No:Z; (g) a nucleotide sequence encoding a mature polypeptide of the amino acid sequence of SEQ ID NO:Y (i.e., a secreted polypeptide (e.g., as delineated in columns 14 and 15 of Table 1A)) or a mature polypeptide of the amino acid sequence encoded by the cDNA in ATCC™ Deposit No:Z; (h) a nucleotide sequence encoding a biologically active fragment of a polypeptide having the complete amino acid sequence of SEQ ID NO:Y or the complete amino acid sequence encoded by the cDNA in ATCC™ Deposit No:Z; (i) a nucleotide sequence encoding an antigenic fragment of a polypeptide having the complete amino acid sequence of SEQ ID NO:Y or the complete amino acid sequence encoded by the cDNA in ATCC™ Deposit No:Z; and (j) a nucleotide sequence complementary to any of the nucleotide sequences in (a), (b), (c), (d), (e), (f), (g), (h), or (i) above.

The present invention is also directed to nucleic acid molecules which comprise, or alternatively consist of, a nucleotide sequence which is at least 80%, 85%, 90%, 95%, 96%, 97%, 98%, 99% or 100%, identical to, for example, any of the nucleotide sequences in (a), (b), (c), (d), (e), (f), (g), (h), (i), or (j) above, the nucleotide coding sequence in SEQ ID NO:X or the complementary strand thereto, the nucleotide coding sequence of the cDNA contained in ATCC™ Deposit No:Z or the complementary strand thereto, a nucleotide sequence encoding the polypeptide of SEQ ID NO:Y, a nucleotide sequence encoding a polypeptide sequence encoded by the nucleotide sequence in SEQ ID NO:X, a polypeptide sequence encoded by the complement of the polynucleotide sequence in SEQ ID NO:X, a nucleotide sequence encoding the polypeptide encoded by the cDNA contained in ATCC™ Deposit No:Z, the nucleotide coding sequence in SEQ ID NO:X as defined in columns 8 and 9 of Table 2 or the complementary strand thereto, a nucleotide sequence encoding the polypeptide encoded by the nucleotide sequence in SEQ ID NO:X as defined in columns 8 and 9 of Table 2 or the complementary strand thereto, the nucleotide coding sequence in SEQ ID NO:B as defined in column 6 of Table 1C or the complementary strand thereto, a nucleotide sequence encoding the polypeptide encoded by the nucleotide sequence in SEQ ID NO:B as defined in column 6 of Table 1C or the complementary strand thereto, the nucleotide sequence in SEQ ID NO:X encoding the polypeptide sequence as defined in columns 6 and 7 of Table 1B.1 or the complementary strand thereto, nucleotide sequences encoding the polypeptide as defined in column 6 and 7 of Table 1B.1 or the complementary strand thereto, and/or polynucleotide fragments of any of these nucleic acid molecules (e.g., those fragments described herein). Polynucleotides which hybridize to the complement of these nucleic acid molecules under stringent hybridization conditions or alternatively, under lower stringency conditions, are also encompassed by the invention, as are polypeptides encoded by these polynucleotides and nucleic acids.

In a preferred embodiment, the invention encompasses nucleic acid molecules which comprise, or alternatively, consist of a polynucleotide which hybridizes under stringent hybridization conditions, or alternatively, under lower stringency conditions, to a polynucleotide in (a), (b), (c), (d), (e), (f), (g), (h), or (i), above, as are polypeptides encoded by these polynucleotides. In another preferred embodiment, polynucleotides which hybridize to the complement of these nucleic acid molecules under stringent hybridization conditions, or alternatively, under lower stringency conditions, are also encompassed by the invention, as are polypeptides encoded by these polynucleotides.

In another embodiment, the invention provides a purified protein comprising, or alternatively consisting of, a polypeptide having an amino acid sequence selected from the group consisting of: (a) the complete amino acid sequence of SEQ ID NO:Y or the complete amino acid sequence encoded by the cDNA in ATCC™ Deposit No:Z; (b) the amino acid sequence of a mature (secreted) form of a polypeptide having the amino acid sequence of SEQ ID NO:Y (e.g., as delineated in columns 14 and 15 of Table 1A) or a mature form of the amino acid sequence encoded by the cDNA in ATCC™ Deposit No:Z mature; (c) the amino acid sequence of a biologically active fragment of a polypeptide having the complete amino acid sequence of SEQ ID NO:Y or the complete amino acid sequence encoded by the cDNA in ATCC™ Deposit No:Z; and (d) the amino acid sequence of an antigenic fragment of a polypeptide having the complete amino acid sequence of SEQ ID NO:Y or the complete amino acid sequence encoded by the cDNA in ATCC™ Deposit No:Z.

The present invention is also directed to proteins which comprise, or alternatively consist of, an amino acid sequence which is at least 80%, 85%, 90%, 95%, 96%, 97%, 98%, 99% or 100%, identical to, for example, any of the amino acid sequences in (a), (b), (c), or (d), above, the amino acid sequence shown in SEQ ID NO:Y, the amino acid sequence encoded by the cDNA contained in ATCC™ Deposit No:Z, the amino acid sequence of the polypeptide encoded by the nucleotide sequence in SEQ ID NO:X as defined in columns 8 and 9 of Table 2, the amino acid sequence of the polypeptide encoded by the nucleotide sequence in SEQ ID NO:B as defined in column 6 of Table 1C, the amino acid sequence as defined in columns 6 and 7 of Table 1B.1, an amino acid sequence encoded by the nucleotide sequence in SEQ ID NO:X, and an amino acid sequence encoded by the complement of the polynucleotide sequence in SEQ ID NO:X. Fragments of these polypeptides are also provided (e.g., those fragments described herein). Further proteins encoded by polynucleotides which hybridize to the complement of the nucleic acid molecules encoding these amino acid sequences under stringent hybridization conditions or alternatively, under lower stringency conditions, are also encompassed by the invention, as are the polynucleotides encoding these proteins.

By a nucleic acid having a nucleotide sequence at least, for example, 95% “identical” to a reference nucleotide sequence of the present invention, it is intended that the nucleotide sequence of the nucleic acid is identical to the reference sequence except that the nucleotide sequence may include up to five point mutations per each 100 nucleotides of the reference nucleotide sequence encoding the polypeptide. In other words, to obtain a nucleic acid having a nucleotide sequence at least 95% identical to a reference nucleotide sequence, up to 5% of the nucleotides in the reference sequence may be deleted or substituted with another nucleotide, or a number of nucleotides up to 5% of the total nucleotides in the reference sequence may be inserted into the reference sequence. The query sequence may be an entire sequence referred to in Table 1B or 2 as the ORF (open reading frame), or any fragment specified as described herein.

As a practical matter, whether any particular nucleic acid molecule or polypeptide is at least 80%, 85%, 90%, 95%, 96%, 97%, 98% or 99% identical to a nucleotide sequence of the present invention can be determined conventionally using known computer programs. A preferred method for determining the best overall match between a query sequence (a sequence of the present invention) and a subject sequence, also referred to as a global sequence alignment, can be determined using the FASTDB computer program based on the algorithm of Brutlag et al. (Comp. App. Biosci. 6:237-245 (1990)). In a sequence alignment the query and subject sequences are both DNA sequences. An RNA sequence can be compared by converting U's to T's. The result of said global sequence alignment is expressed as percent identity. Preferred parameters used in a FASTDB alignment of DNA sequences to calculate percent identity are: Matrix=Unitary, k-tuple=4, Mismatch Penalty=1, Joining Penalty=30, Randomization Group Length=0, Cutoff Score=1, Gap Penalty=5, Gap Size Penalty 0.05, Window Size=500 or the length of the subject nucleotide sequence, whichever is shorter.

If the subject sequence is shorter than the query sequence because of 5′ or 3′ deletions, not because of internal deletions, a manual correction must be made to the results. This is because the FASTDB program does not account for 5′ and 3′ truncations of the subject sequence when calculating percent identity. For subject sequences truncated at the 5′ or 3′ ends, relative to the query sequence, the percent identity is corrected by calculating the number of bases of the query sequence that are 5′ and 3′ of the subject sequence, which are not matched/aligned, as a percent of the total bases of the query sequence. Whether a nucleotide is matched/aligned is determined by results of the FASTDB sequence alignment. This percentage is then subtracted from the percent identity, calculated by the above FASTDB program using the specified parameters, to arrive at a final percent identity score. This corrected score is what is used for the purposes of the present invention. Only bases outside the 5′ and 3′ bases of the subject sequence, as displayed by the FASTDB alignment, which are not matched/aligned with the query sequence, are calculated for the purposes of manually adjusting the percent identity score.

For example, a 90 base subject sequence is aligned to a 100 base query sequence to determine percent identity. The deletions occur at the 5′ end of the subject sequence and therefore, the FASTDB alignment does not show a matched/alignment of the first 10 bases at 5′ end. The 10 unpaired bases represent 10% of the sequence (number of bases at the 5′ and 3′ ends not matched/total number of bases in the query sequence) so 10% is subtracted from the percent identity score calculated by the FASTDB program. If the remaining 90 bases were perfectly matched the final percent identity would be 90%. In another example, a 90 base subject sequence is compared with a 100 base query sequence. This time the deletions are internal deletions so that there are no bases on the 5′ or 3′ of the subject sequence which are not matched/aligned with the query. In this case the percent identity calculated by FASTDB is not manually corrected. Once again, only bases 5′ and 3′ of the subject sequence which are not matched/aligned with the query sequence are manually corrected for. No other manual corrections are to be made for the purposes of the present invention.

By a polypeptide having an amino acid sequence at least, for example, 95% “identical” to a query amino acid sequence of the present invention, it is intended that the amino acid sequence of the subject polypeptide is identical to the query sequence except that the subject polypeptide sequence may include up to five amino acid alterations per each 100 amino acids of the query amino acid sequence. In other words, to obtain a polypeptide having an amino acid sequence at least 95% identical to a query amino acid sequence, up to 5% of the amino acid residues in the subject sequence may be inserted, deleted, (indels) or substituted with another amino acid. These alterations of the reference sequence may occur at the amino or carboxy terminal positions of the reference amino acid sequence or anywhere between those terminal positions, interspersed either individually among residues in the reference sequence or in one or more contiguous groups within the reference sequence.

As a practical matter, whether any particular polypeptide is at least 80%, 85%, 90%, 95%, 96%, 97%, 98% or 99% identical to, for instance, the amino acid sequence of a polypeptide referred to in Table 1A (e.g., the amino acid sequence delineated in columns 14 and 15) or a fragment thereof, Table 1B.1 (e.g., the amino acid sequence identified in column 6) or a fragment thereof, Table 2 (e.g., the amino acid sequence of the polypeptide encoded by the polynucleotide sequence defined in columns 8 and 9 of Table 2) or a fragment thereof, the amino acid sequence of the polypeptide encoded by the polynucleotide sequence in SEQ ID NO:B as defined in column 6 of Table 1C or a fragment thereof, the amino acid sequence of the polypeptide encoded by the nucleotide sequence in SEQ ID NO:X or a fragment thereof, or the amino acid sequence of the polypeptide encoded by cDNA contained in ATCC™ Deposit No:Z, or a fragment thereof, the amino acid sequence of a mature (secreted) polypeptide encoded by cDNA contained in ATCC™ Deposit No:Z, or a fragment thereof, can be determined conventionally using known computer programs. A preferred method for determining the best overall match between a query sequence (a sequence of the present invention) and a subject sequence, also referred to as a global sequence alignment, can be determined using the FASTDB computer program based on the algorithm of Brutlag et al. (Comp. App. Biosci.6:237-245 (1990)). In a sequence alignment the query and subject sequences are either both nucleotide sequences or both amino acid sequences. The result of said global sequence alignment is expressed as percent identity. Preferred parameters used in a FASTDB amino acid alignment are: Matrix=PAM 0, k-tuple=2, Mismatch Penalty=1, Joining Penalty=20, Randomization Group Length=0, Cutoff Score=1, Window Size=sequence length, Gap Penalty=5, Gap Size Penalty=0.05, Window Size=500 or the length of the subject amino acid sequence, whichever is shorter.

If the subject sequence is shorter than the query sequence due to N- or C-terminal deletions, not because of internal deletions, a manual correction must be made to the results. This is because the FASTDB program does not account for N- and C-terminal truncations of the subject sequence when calculating global percent identity. For subject sequences truncated at the N- and C-termini, relative to the query sequence, the percent identity is corrected by calculating the number of residues of the query sequence that are N- and C-terminal of the subject sequence, which are not matched/aligned with a corresponding subject residue, as a percent of the total bases of the query sequence. Whether a residue is matched/aligned is determined by results of the FASTDB sequence alignment. This percentage is then subtracted from the percent identity, calculated by the above FASTDB program using the specified parameters, to arrive at a final percent identity score. This final percent identity score is what is used for the purposes of the present invention. Only residues to the N- and C-termini of the subject sequence, which are not matched/aligned with the query sequence, are considered for the purposes of manually adjusting the percent identity score. That is, only query residue positions outside the farthest N- and C-terminal residues of the subject sequence.

For example, a 90 amino acid residue subject sequence is aligned with a 100 residue query sequence to determine percent identity. The deletion occurs at the N-terminus of the subject sequence and therefore, the FASTDB alignment does not show a matching/alignment of the first 10 residues at the N-terminus. The 10 unpaired residues represent 10% of the sequence (number of residues at the N- and C-termini not matched/total number of residues in the query sequence) so 10% is subtracted from the percent identity score calculated by the FASTDB program. If the remaining 90 residues were perfectly matched the final percent identity would be 90%. In another example, a 90 residue subject sequence is compared with a 100 residue query sequence. This time the deletions are internal deletions so there are no residues at the N- or C-termini of the subject sequence which are not matched/aligned with the query. In this case the percent identity calculated by FASTDB is not manually corrected. Once again, only residue positions outside the N- and C-terminal ends of the subject sequence, as displayed in the FASTDB alignment, which are not matched/aligned with the query sequence are manually corrected for. No other manual corrections are to made for the purposes of the present invention.

The polynucleotide variants of the invention may contain alterations in the coding regions, non-coding regions, or both. Especially preferred are polynucleotide variants containing alterations which produce silent substitutions, additions, or deletions, but do not alter the properties or activities of the encoded polypeptide. Nucleotide variants produced by silent substitutions due to the degeneracy of the genetic code are preferred. Moreover, polypeptide variants in which less than 50, less than 40, less than 30, less than 20, less than 10, or 5-50, 5-25, 5-10, 1-5, or 1-2 amino acids are substituted, deleted, or added in any combination are also preferred. Polynucleotide variants can be produced for a variety of reasons, e.g., to optimize codon expression for a particular host (change codons in the human mRNA to those preferred by a bacterial host such as E. coli).

Naturally occurring variants are called “allelic variants,” and refer to one of several alternate forms of a gene occupying a given locus on a chromosome of an organism. (Genes II, Lewin, B., ed., John Wiley & Sons, New York (1985)). These allelic variants can vary at either the polynucleotide and/or polypeptide level and are included in the present invention. Alternatively, non-naturally occurring variants may be produced by mutagenesis techniques or by direct synthesis.

Using known methods of protein engineering and recombinant DNA technology, variants may be generated to improve or alter the characteristics of the polypeptides of the present invention. For instance, one or more amino acids can be deleted from the N-terminus or C-terminus of the polypeptide of the present invention without substantial loss of biological function. As an example, Ron et al. (J. Biol. Chem. 268: 2984-2988 (1993)) reported variant KGF proteins having heparin binding activity even after deleting 3, 8, or 27 amino-terminal amino acid residues. Similarly, Interferon gamma exhibited up to ten times higher activity after deleting 8-10 amino acid residues from the carboxy terminus of this protein. (Dobeli et al., J. Biotechnology 7:199-216 (1988).)

Moreover, ample evidence demonstrates that variants often retain a biological activity similar to that of the naturally occurring protein. For example, Gayle and coworkers (J. Biol. Chem. 268:22105-22111 (1993)) conducted extensive mutational analysis of human cytokine IL-1a. They used random mutagenesis to generate over 3,500 individual IL-1a mutants that averaged 2.5 amino acid changes per variant over the entire length of the molecule. Multiple mutations were examined at every possible amino acid position. The investigators found that “[m]ost of the molecule could be altered with little effect on either [binding or biological activity].” In fact, only 23 unique amino acid sequences, out of more than 3,500 nucleotide sequences examined, produced a protein that significantly differed in activity from wild-type.

Furthermore, even if deleting one or more amino acids from the N-terminus or C-terminus of a polypeptide results in modification or loss of one or more biological functions, other biological activities may still be retained. For example, the ability of a deletion variant to induce and/or to bind antibodies which recognize the secreted form will likely be retained when less than the majority of the residues of the secreted form are removed from the N-terminus or C-terminus. Whether a particular polypeptide lacking N- or C-terminal residues of a protein retains such immunogenic activities can readily be determined by routine methods described herein and otherwise known in the art.

Thus, the invention further includes polypeptide variants which show a biological or functional activity of the polypeptides of the invention (such as, for example, activity useful in detecting, preventing, diagnosing, prognosticating, treating, and/or ameliorating cardiovascular disorders). Such variants include deletions, insertions, inversions, repeats, and substitutions selected according to general rules known in the art so as have little effect on activity.

The present application is directed to nucleic acid molecules at least 80%, 85%, 90%, 95%, 96%, 97%, 98%, 99% or 100% identical to the nucleic acid sequences disclosed herein, (e.g., encoding a polypeptide having the amino acid sequence of an N and/or C terminal deletion), irrespective of whether they encode a polypeptide having functional activity. This is because even where a particular nucleic acid molecule does not encode a polypeptide having functional activity, one of skill in the art would still know how to use the nucleic acid molecule, for instance, as a hybridization probe or a polymerase chain reaction (PCR) primer. Uses of the nucleic acid molecules of the present invention that do not encode a polypeptide having functional activity include, inter alia, (1) isolating a gene or allelic or splice variants thereof in a cDNA library; (2) in situ hybridization (e.g., “FISH”) to metaphase chromosomal spreads to provide precise chromosomal location of the gene, as described in Verma et al., Human Chromosomes: A Manual of Basic Techniques, Pergamon Press, New York (1988); (3) Northern Blot analysis for detecting mRNA expression in specific tissues (e.g., normal or diseased tissues); and (4) in situ hybridization (e.g., histochemistry) for detecting mRNA expression in specific tissues (e.g., normal or diseased tissues).

Preferred, however, are nucleic acid molecules having sequences at least 80%, 85%, 90%, 95%, 96%, 97%, 98%, 99% or 100% identical to the nucleic acid sequences disclosed herein, which do, in fact, encode a polypeptide having functional activity. By a polypeptide having “functional activity” is meant, a polypeptide capable of displaying one or more known functional activities associated with a full-length (complete) protein and/or a mature (secreted) protein of the invention. Such functional activities include, but are not limited to, biological activity (such as, for example, activity useful in detecting, preventing, diagnosing, prognosticating, treating, and/or ameliorating cancer and other hyperproliferative diseases and disorders), antigenicity (ability to bind, or compete with a polypeptide of the invention for binding, to an anti-polypeptide of the invention antibody), immunogenicity (ability to generate antibody which binds to a specific polypeptide of the invention), ability to form multimers with polypeptides of the invention, and ability to bind to a receptor or ligand for a polypeptide of the invention.

The functional activity of the polypeptides, and fragments, variants and derivatives of the invention, can be assayed by various methods.

For example, in one embodiment where one is assaying for the ability to bind or compete with a full-length polypeptide of the present invention for binding to an anti-polypeptide antibody, various immunoassays known in the art can be used, including but not limited to, competitive and non-competitive assay systems using techniques such as radioimmunoassays, ELISA (enzyme linked immunosorbent assay), “sandwich” immunoassays, immunoradiometric assays, gel diffusion precipitation reactions, immunodiffusion assays, in situ immunoassays (using colloidal gold, enzyme or radioisotope labels, for example), western blots, precipitation reactions, agglutination assays (e.g., gel agglutination assays, hemagglutination assays), complement fixation assays, immunofluorescence assays, protein A assays, and immunoelectrophoresis assays, etc. In one embodiment, antibody binding is detected by detecting a label on the primary antibody. In another embodiment, the primary antibody is detected by detecting binding of a secondary antibody or reagent to the primary antibody. In a further embodiment, the secondary antibody is labeled. Many means are known in the art for detecting binding in an immunoassay and are within the scope of the present invention.

In another embodiment, where a ligand is identified, or the ability of a polypeptide fragment, variant or derivative of the invention to multimerize is being evaluated, binding can be assayed, e.g., by means well-known in the art, such as, for example, reducing and non-reducing gel chromatography, protein affinity chromatography, and affinity blotting. See generally, Phizicky et al., Microbiol. Rev. 59:94-123 (1995). In another embodiment, the ability of physiological correlates of a polypeptide of the present invention to bind to a substrate(s) of the polypeptide of the invention can be routinely assayed using techniques known in the art.

In addition, assays described herein (see Examples) and otherwise known in the art may routinely be applied to measure the ability of polypeptides of the present invention and fragments, variants and derivatives thereof to elicit polypeptide related biological activity (either in vitro or in vivo). Other methods will be known to the skilled artisan and are within the scope of the invention.

Of course, due to the degeneracy of the genetic code, one of ordinary skill in the art will immediately recognize that a large number of the nucleic acid molecules having a sequence at least 80%, 85%, 90%, 95%, 96%, 97%, 98%, 99%, or 100% identical to, for example, the nucleic acid sequence of the cDNA contained in ATCC™ Deposit No:Z, the nucleic acid sequence referred to in Table 1B (SEQ ID NO:X), the nucleic acid sequence disclosed in Table 1A (e.g., the nucleic acid sequence delineated in columns 7 and 8), the nucleic acid sequence disclosed in Table 2 (e.g., the nucleic acid sequence delineated in columns 8 and 9) or fragments thereof, will encode polypeptides “having functional activity.” In fact, since degenerate variants of any of these nucleotide sequences all encode the same polypeptide, in many instances, this will be clear to the skilled artisan even without performing the above described comparison assay. It will be further recognized in the art that, for such nucleic acid molecules that are not degenerate variants, a reasonable number will also encode a polypeptide having functional activity. This is because the skilled artisan is fully aware of amino acid substitutions that are either less likely or not likely to significantly effect protein function (e.g., replacing one aliphatic amino acid with a second aliphatic amino acid), as further described below.

For example, guidance concerning how to make phenotypically silent amino acid substitutions is provided in Bowie et al., “Deciphering the Message in Protein Sequences: Tolerance to Amino Acid Substitutions,” Science 247:1306-1310 (1990), wherein the authors indicate that there are two main strategies for studying the tolerance of an amino acid sequence to change.

The first strategy exploits the tolerance of amino acid substitutions by natural selection during the process of evolution. By comparing amino acid sequences in different species, conserved amino acids can be identified. These conserved amino acids are likely important for protein function. In contrast, the amino acid positions where substitutions have been tolerated by natural selection indicates that these positions are not critical for protein function. Thus, positions tolerating amino acid substitution could be modified while still maintaining biological activity of the protein.

The second strategy uses genetic engineering to introduce amino acid changes at specific positions of a cloned gene to identify regions critical for protein function. For example, site directed mutagenesis or alanine-scanning mutagenesis (introduction of single alanine mutations at every residue in the molecule) can be used. See Cunningham and Wells, Science 244:1081-1085 (1989). The resulting mutant molecules can then be tested for biological activity.

As the authors state, these two strategies have revealed that proteins are surprisingly tolerant of amino acid substitutions. The authors further indicate which amino acid changes are likely to be permissive at certain amino acid positions in the protein. For example, most buried (within the tertiary structure of the protein) amino acid residues require nonpolar side chains, whereas few features of surface side chains are generally conserved. Moreover, tolerated conservative amino acid substitutions involve replacement of the aliphatic or hydrophobic amino acids Ala, Val, Leu and Ile; replacement of the hydroxyl residues Ser and Thr; replacement of the acidic residues Asp and Glu; replacement of the amide residues Asn and Gln, replacement of the basic residues Lys, Arg, and His; replacement of the aromatic residues Phe, Tyr, and Trp, and replacement of the small-sized amino acids Ala, Ser, Thr, Met, and Gly.

Besides conservative amino acid substitution, variants of the present invention include (i) substitutions with one or more of the non-conserved amino acid residues, where the substituted amino acid residues may or may not be one encoded by the genetic code, or (ii) substitutions with one or more of the amino acid residues having a substituent group, or (iii) fusion of the mature polypeptide with another compound, such as a compound to increase the stability and/or solubility of the polypeptide (for example, polyethylene glycol), (iv) fusion of the polypeptide with additional amino acids, such as, for example, an IgG Fc fusion region peptide, serum albumin (preferably human serum albumin) or a fragment thereof, or leader or secretory sequence, or a sequence facilitating purification, or (v) fusion of the polypeptide with another compound, such as albumin (including but not limited to recombinant albumin (see, e.g., U.S. Pat. No. 5,876,969, issued Mar. 2, 1999, EP Patent 0 413 622, and U.S. Pat. No. 5,766,883, issued Jun. 16, 1998, herein incorporated by reference in their entirety)). Such variant polypeptides are deemed to be within the scope of those skilled in the art from the teachings herein.

For example, polypeptide variants containing amino acid substitutions of charged amino acids with other charged or neutral amino acids may produce proteins with improved characteristics, such as less aggregation. Aggregation of pharmaceutical formulations both reduces activity and increases clearance due to the aggregate's immunogenic activity. See Pinckard et al., Clin. Exp. Immunol. 2:331-340 (1967); Robbins et al., Diabetes 36: 838-845 (1987); Cleland et al., Crit. Rev. Therapeutic Drug Carrier Systems 10:307-377 (1993).

A further embodiment of the invention relates to polypeptides which comprise the amino acid sequence of a polypeptide having an amino acid sequence which contains at least one amino acid substitution, but not more than 50 amino acid substitutions, even more preferably, not more than 40 amino acid substitutions, still more preferably, not more than 30 amino acid substitutions, and still even more preferably, not more than 20 amino acid substitutions from a polypeptide sequence disclosed herein. Of course it is highly preferable for a polypeptide to have an amino acid sequence which, for example, comprises the amino acid sequence of a polypeptide of SEQ ID NO:Y, the amino acid sequence of the mature (e.g., secreted) polypeptide of SEQ ID NO:Y, an amino acid sequence encoded by SEQ ID NO:X, an amino acid sequence encoded by the portion of SEQ ID NO:X as defined in columns 8 and 9 of Table 2, an amino acid sequence encoded by the complement of SEQ ID NO:X, an amino acid sequence encoded by cDNA contained in ATCC™ Deposit No:Z, and/or the amino acid sequence of a mature (secreted) polypeptide encoded by cDNA contained in ATCC™ Deposit No:Z, or a fragment thereof, which contains, in order of ever-increasing preference, at least one, but not more than 10, 9, 8, 7, 6, 5, 4, 3, 2 or 1 amino acid substitutions.

In specific embodiments, the polypeptides of the invention comprise, or alternatively, consist of, fragments or variants of a reference amino acid sequence selected from: (a) the amino acid sequence of SEQ ID NO:Y or fragments thereof (e.g., the mature form and/or other fragments described herein); (b) the amino acid sequence encoded by SEQ ID NO:X or fragments thereof; (c) the amino acid sequence encoded by the complement of SEQ ID NO:X or fragments thereof; (d) the amino acid sequence encoded by the portion of SEQ ID NO:X as defined in columns 8 and 9 of Table 2 or fragments thereof; and (e) the amino acid sequence encoded by cDNA contained in ATCC™ Deposit No:Z or fragments thereof; wherein the fragments or variants have 1-5, 5-10, 5-25, 5-50, 10-50 or 50-150, amino acid residue additions, substitutions, and/or deletions when compared to the reference amino acid sequence. In preferred embodiments, the amino acid substitutions are conservative. Polynucleotides encoding these polypeptides are also encompassed by the invention.

Polynucleotide and Polypeptide Fragments

The present invention is also directed to polynucleotide fragments of the polynucleotides (nucleic acids) of the invention. In the present invention, a “polynucleotide fragment” refers to a polynucleotide having a nucleic acid sequence which, for example: is a portion of the cDNA contained in ATCC™ Deposit No:Z or the complementary strand thereto; is a portion of the polynucleotide sequence encoding the polypeptide encoded by the cDNA contained in ATCC™ Deposit No:Z or the complementary strand thereto; is a portion of the polynucleotide sequence encoding the mature (secreted) polypeptide encoded by the cDNA contained in ATCC™ Deposit No:Z or the complementary strand thereto; is a portion of a polynucleotide sequence encoding the mature amino acid sequence as defined in columns 14 and 15 of Table 1A or the complementary strand thereto; is a portion of a polynucleotide sequence encoding the amino acid sequence encoded by the region of SEQ ID NO:X as defined in columns 8 and 9 of Table 2 or the complementary strand thereto; is a portion of the polynucleotide sequence of SEQ ID NO:X as defined in columns 8 and 9 of Table 2 or the complementary strand thereto; is a portion of the polynucleotide sequence in SEQ ID NO:X or the complementary strand thereto; is a polynucleotide sequence encoding a portion of the polypeptide of SEQ ID NO:Y; is a polynucleotide sequence encoding a portion of a polypeptide encoded by SEQ ID NO:X; is a polynucleotide sequence encoding a portion of a polypeptide encoded by the complement of the polynucleotide sequence in SEQ ID NO:X; is a portion of a polynucleotide sequence encoding the amino acid sequence encoded by the region of SEQ ID NO:B as defined in column 6 of Table 1C or the complementary strand thereto; or is a portion of the polynucleotide sequence of SEQ ID NO:B as defined in column 6 of Table 1C or the complementary strand thereto.

The polynucleotide fragments of the invention are preferably at least about 15 nt, and more preferably at least about 20 nt, still more preferably at least about 30 nt, and even more preferably, at least about 40 nt, at least about 50 nt, at least about 75 nt, or at least about 150 nt in length. A fragment “at least 20 nt in length,” for example, is intended to include 20 or more contiguous bases from the cDNA sequence contained in ATCC™ Deposit No:Z, or the nucleotide sequence shown in SEQ ID NO:X or the complementary stand thereto. In this context “about” includes the particularly recited value or a value larger or smaller by several (5, 4, 3, 2, or 1) nucleotides, at either terminus or at both termini. These nucleotide fragments have uses that include, but are not limited to, as diagnostic probes and primers as discussed herein. Of course, larger fragments (e.g., at least 160, 170, 180, 190, 200, 250, 500, 600, 1000, or 2000 nucleotides in length) are also encompassed by the invention.

Moreover, representative examples of polynucleotide fragments of the invention comprise, or alternatively consist of, a sequence from about nucleotide number 1-50, 51-100, 101-150, 151-200, 201-250, 251-300, 301-350, 351-400, 401-450, 451-500, 501-550, 551-600, 601-650, 651-700, 701-750, 751-800, 801-850, 851-900, 901-950, 951-1000, 1001-1050, 1051-1100, 1101-1150, 1151-1200, 1201-1250, 1251-1300, 1301-1350, 1351-1400, 1401-1450, 1451-1500, 1501-1550, 1551-1600, 1601-1650, 1651-1700, 1701-1750, 1751-1800, 1801-1850, 1851-1900, 1901-1950, 1951-2000, 2001-2050, 2051-2100, 2101-2150, 2151-2200, 2201-2250, 2251-2300, 2301-2350, 2351-2400, 2401-2450, 2451-2500, 2501-2550, 2551-2600, 2601-2650, 2651-2700, 2701-2750, 2751-2800, 2801-2850, 2851-2900, 2901-2950, 2951-3000, 3001-3050, 3051-3100, 3101-3150, 3151-3200, 3201-3250, 3251-3300, 3301-3350, 3351-3400, 3401-3450, 3451-3500, 3501-3550, 3551-3600, 3601-3650, 3651-3700, 3701-3750, 3751-3800, 3801-3850, 3851-3900, 3901-3950, 3951-4000, 4001-4050, 4051-4100, 4101-4150, 4151-4200, 4201-4250, 4251-4300, 4301-4350, 4351-4400, 4401-4450, 4451-4500, 4501-4550, 4551-4600, 4601-4650, 4651-4700, 4701-4750, 4751-4800, 4801-4850, 4851-4900, 4901-4950, 4951-5000, 5001-5050, 5051-5100, 5101-5150, 5151-5200, 5201-5250, 5251-5300, 5301-5350, 5351-5400, 5401-5450, 5451-5500, 5501-5550, 5551-5600, 5601-5650, 5651-5700, 5701-5750, 5751-5800, 5801-5850, 5851-5900, 5901-5950, 5951-6000, 6001-6050, 6051-6100, 6101-6150, 6151-6200, 6201-6250, 6251-6300, 6301-6350, 6351-6400, 6401-6450, 6451-6500, 6501-6550, 6551-6600, 6601-6650, 6651-6700, 6701-6750, 6751-6800, 6801-6850, 6851-6900, 6901-6950, 6951-7000, 7001-7050, 7051-7100, 7101-7150, 7151-7200, 7201-7250, 7251-7300 or 7301 to the end of SEQ ID NO:X, or the complementary strand thereto. In this context “about” includes the particularly recited range or a range larger or smaller by several (5, 4, 3, 2, or 1) nucleotides, at either terminus or at both termini. Preferably, these fragments encode a polypeptide which has a functional activity (e.g., biological activity; such as, for example, activity useful in detecting, preventing, diagnosing, prognosticating, treating, and/or ameliorating cancer and other hyperproliferative diseases and disorders). More preferably, these polynucleotides can be used as probes or primers as discussed herein. Polynucleotides which hybridize to one or more of these polynucleotides under stringent hybridization conditions or alternatively, under lower stringency conditions are also encompassed by the invention, as are polypeptides encoded by these polynucleotides.

Further representative examples of polynucleotide fragments of the invention comprise, or alternatively consist of, a sequence from about nucleotide number 1-50, 51-100, 101-150, 151-200, 201-250, 251-300, 301-350, 351-400, 401-450, 451-500, 501-550, 551-600, 601-650, 651-700, 701-750, 751-800, 801-850, 851-900, 901-950, 951-1000, 1001-1050, 1051-1100, 1101-1150, 1151-1200, 1201-1250, 1251-1300, 1301-1350, 1351-1400, 1401-1450, 1451-1500, 1501-1550, 1551-1600, 1601-1650, 1651-1700, 1701-1750, 1751-1800, 1801-1850, 1851-1900, 1901-1950, 1951-2000, 2001-2050, 2051-2100, 2101-2150, 2151-2200, 2201-2250, 2251-2300, 2301-2350, 2351-2400, 2401-2450, 2451-2500, 2501-2550, 2551-2600, 2601-2650, 2651-2700, 2701-2750, 2751-2800, 2801-2850, 2851-2900, 2901-2950, 2951-3000, 3001-3050, 3051-3100, 3101-3150, 3151-3200, 3201-3250, 3251-3300, 3301-3350, 3351-3400, 3401-3450, 3451-3500, 3501-3550, 3551-3600, 3601-3650, 3651-3700, 3701-3750, 3751-3800, 3801-3850, 3851-3900, 3901-3950, 3951-4000, 4001-4050, 4051-4100, 4101-4150, 4151-4200, 4201-4250, 4251-4300, 4301-4350, 4351-4400, 4401-4450, 4451-4500, 4501-4550, 4551-4600, 4601-4650, 4651-4700, 4701-4750, 4751-4800, 4801-4850, 4851-4900, 4901-4950, 4951-5000, 5001-5050, 5051-5100, 5101-5150, 5151-5200, 5201-5250, 5251-5300, 5301-5350, 5351-5400, 5401-5450, 5451-5500, 5501-5550, 5551-5600, 5601-5650, 5651-5700, 5701-5750, 5751-5800, 5801-5850, 5851-5900, 5901-5950, 5951-6000, 6001-6050, 6051-6100, 6101-6150, 6151-6200, 6201-6250, 6251-6300, 6301-6350, 6351-6400, 6401-6450, 6451-6500, 6501-6550, 6551-6600, 6601-6650, 6651-6700, 6701-6750, 6751-6800, 6801-6850, 6851-6900, 6901-6950, 6951-7000, 7001-7050, 7051-7100, 7101-7150, 7151-7200, 7201-7250, 7251-7300 or 7301 to the end of the cDNA sequence contained in ATCC™ Deposit No:Z, or the complementary strand thereto. In this context “about” includes the particularly recited range or a range larger or smaller by several (5, 4, 3, 2, or 1) nucleotides, at either terminus or at both termini. Preferably, these fragments encode a polypeptide which has a functional activity (e.g., biological activity). More preferably, these polynucleotides can be used as probes or primers as discussed herein. Polynucleotides which hybridize to one or more of these polynucleotides under stringent hybridization conditions or alternatively, under lower stringency conditions are also encompassed by the invention, as are polypeptides encoded by these polynucleotides.

Moreover, representative examples of polynucleotide fragments of the invention comprise, or alternatively consist of, a nucleic acid sequence comprising one, two, three, four, five, six, seven, eight, nine, ten, or more of the above described polynucleotide fragments of the invention in combination with a polynucleotide sequence delineated in Table 1C column 6. Additional, representative examples of polynucleotide fragments of the invention comprise, or alternatively consist of, a nucleic acid sequence comprising one, two, three, four, five, six, seven, eight, nine, ten, or more of the above described polynucleotide fragments of the invention in combination with a polynucleotide sequence that is the complementary strand of a sequence delineated in column 6 of Table 1C. In further embodiments, the above-described polynucleotide fragments of the invention comprise, or alternatively consist of, sequences delineated in Table 1C, column 6, and have a nucleic acid sequence which is different from that of the BAC fragment having the sequence disclosed in SEQ ID NO:B (see Table 1C, column 5). In additional embodiments, the above-described polynucleotide fragments of the invention comprise, or alternatively consist of, sequences delineated in Table 1C, column 6, and have a nucleic acid sequence which is different from that published for the BAC clone identified as BAC ID NO:A (see Table 1C, column 4). In additional embodiments, the above-described polynucleotides of the invention comprise, or alternatively consist of, sequences delineated Table 1C, column 6, and have a nucleic acid sequence which is different from that contained in the BAC clone identified as BAC ID NO:A (see Table 1C, column 4). Polypeptides encoded by these polynucleotides, other polynucleotides that encode these polypeptides, and antibodies that bind these polypeptides are also encompassed by the invention. Additionally, fragments and variants of the above-described polynucleotides and polypeptides are also encompassed by the invention.

In additional specific embodiments, polynucleotides of the invention comprise, or alternatively consist of, one, two, three, four, five, six, seven, eight, nine, ten, or more fragments of the sequences delineated in column 6 of Table 1C, and the polynucleotide sequence of SEQ ID NO:X (e.g., as defined in Table 1C, column 2) or fragments or variants thereof. Polypeptides encoded by these polynucleotides, other polynucleotides that encode these polypeptides, and antibodies that bind these polypeptides are also encompassed by the invention.

In additional specific embodiments, polynucleotides of the invention comprise, or alternatively consist of, one, two, three, four, five, six, seven, eight, nine, ten, or more fragments of the sequences delineated in column 6 of Table 1C which correspond to the same ATCC™ Deposit No:Z (see Table 1C, column 1), and the polynucleotide sequence of SEQ ID NO:X (e.g., as defined in Table 1A, 1B, or 1C) or fragments or variants thereof. Polypeptides encoded by these polynucleotides, other polynucleotides that encode these polypeptides, and antibodies that bind these polypeptides are also encompassed by the invention.

In further specific embodiments, polynucleotides of the invention comprise, or alternatively consist of, one, two, three, four, five, six, seven, eight, nine, ten, or more fragments of the sequences delineated in the same row of column 6 of Table 1C, and the polynucleotide sequence of SEQ ID NO:X (e.g., as defined in Table 1A, 1B, or 1C) or fragments or variants thereof. Polypeptides encoded by these polynucleotides, other polynucleotides that encode these polypeptides, and antibodies that bind these polypeptides are also encompassed by the invention.

In additional specific embodiments, polynucleotides of the invention comprise, or alternatively consist of a polynucleotide sequence in which the 3′ 10 polynucleotides of one of the sequences delineated in column 6 of Table 1C and the 5′ 10 polynucleotides of the sequence of SEQ ID NO:X are directly contiguous. Nucleic acids which hybridize to the complement of these 20 contiguous polynucleotides under stringent hybridization conditions or alternatively, under lower stringency conditions, are also encompassed by the invention. Polypeptides encoded by these polynucleotides and/or nucleic acids, other polynucleotides and/or nucleic acids that encode these polypeptides, and antibodies that bind these polypeptides are also encompassed by the invention. Additionally, fragments and variants of the above-described polynucleotides, nucleic acids, and polypeptides are also encompassed by the invention.

In additional specific embodiments, polynucleotides of the invention comprise, or alternatively consist of a polynucleotide sequence in which the 3′ 10 polynucleotides of one of the sequences delineated in column 6 of Table 1C and the 5′ 10 polynucleotides of a fragment or variant of the sequence of SEQ ID NO:X (e.g., as described herein) are directly contiguous Nucleic acids which hybridize to the complement of these 20 contiguous polynucleotides under stringent hybridization conditions or alternatively, under lower stringency conditions, are also encompassed by the invention. Polypeptides encoded by these polynucleotides and/or nucleic acids, other polynucleotides and/or nucleic acids encoding these polypeptides, and antibodies that bind these polypeptides are also encompassed by the invention. Additionally, fragments and variants of the above-described polynucleotides, nucleic acids, and polypeptides are also encompassed by the invention.

In further specific embodiments, polynucleotides of the invention comprise, or alternatively consist of a polynucleotide sequence in which the 3′ 10 polynucleotides of a fragment or variant of the sequence of SEQ ID NO:X and the 5′ 10 polynucleotides of the sequence of one of the sequences delineated in column 6 of Table 1C are directly contiguous. Nucleic acids which hybridize to the complement of these 20 contiguous polynucleotides under stringent hybridization conditions or alternatively, under lower stringency conditions, are also encompassed by the invention. Polypeptides encoded by these polynucleotides and/or nucleic acids, other polynucleotides and/or nucleic acids encoding these polypeptides, and antibodies that bind these polypeptides are also encompassed by the invention. Additionally, fragments and variants of the above-described polynucleotides, nucleic acids, and polypeptides are also encompassed by the invention.

In specific embodiments, polynucleotides of the invention comprise, or alternatively consist of a polynucleotide sequence in which the 3′ 10 polynucleotides of one of the sequences delineated in column 6 of Table 1C and the 5′ 10 polynucleotides of another sequence in column 6 are directly contiguous. In preferred embodiments, the 3′ 10 polynucleotides of one of the sequences delineated in column 6 of Table 1C is directly contiguous with the 5′ 10 polynucleotides of the next sequential exon delineated in Table 1C, column 6. Nucleic acids which hybridize to the complement of these 20 contiguous polynucleotides under stringent hybridization conditions or alternatively, under lower stringency conditions, are also encompassed by the invention. Polypeptides encoded by these polynucleotides and/or nucleic acids, other polynucleotides and/or nucleic acids encoding these polypeptides, and antibodies that bind these polypeptides are also encompassed by the invention. Additionally, fragments and variants of the above-described polynucleotides, nucleic acids, and polypeptides are also encompassed by the invention.

In the present invention, a “polypeptide fragment” refers to an amino acid sequence which is a portion of the amino acid sequence contained in SEQ ID NO:Y, is a portion of the mature form of SEQ ID NO:Y as defined in columns 14 and 15 of Table 1A, a portion of an amino acid sequence encoded by the portion of SEQ ID NO:X as defined in columns 8 and 9 of Table 2, is a portion of an amino acid sequence encoded by the polynucleotide sequence of SEQ ID NO:X, is a portion of an amino acid sequence encoded by the complement of the polynucleotide sequence in SEQ ID NO:X, is a portion of the amino acid sequence of a mature (secreted) polypeptide encoded by the cDNA contained in ATCC™ Deposit No:Z, and/or is a portion of an amino acid sequence encoded by the cDNA contained in ATCC™ Deposit No:Z. Protein (polypeptide) fragments may be “free-standing,” or comprised within a larger polypeptide of which the fragment forms a part or region, most preferably as a single continuous region. Representative examples of polypeptide fragments of the invention, include, for example, fragments comprising, or alternatively consisting of, from about amino acid number 1-20, 21-40, 41-60, 61-80, 81-100, 101-120, 121-140, 141-160, 161-180, 181-200, 201-220, 221-240, 241-260, 261-280, 281-300, 301-320, 321-340, 341-360, 361-380, 381-400, 401-420, 421-440, 441-460, 461-480, 481-500, 501-520, 521-540, 541-560, 561-580, 581-600, 601-620, 621-640, 641-660, 661-680, 681-700, 701-720, 721-740, 741-760, 761-780, 781-800, 801-820, 821-840, 841-860, 861-880, 881-900, 901-920, 921-940, 941-960, 961-980, 981-1000, 1001-1020, 1021-1040, 1041-1060, 1061-1080, 1081-1100, 1101-1120, 1121-1140, 1141-1160, 1161-1180, 1181-1200, 1201-1220, 1221-1240, 1241-1260, 1261-1280, 1281-1300, 1301-1320, 1321-1340, 1341-1360, 1361-1380, 1381-1400, 1401-1420, 1421-1440, or 1441 to the end of the coding region of cDNA and SEQ ID NO: Y. In a preferred embodiment, polypeptide fragments of the invention include, for example, fragments comprising, or alternatively consisting of, from about amino acid number 1-20, 21-40, 41-60, 61-80, 81-100, 101-120, 121-140, 141-160, 161-180, 181-200, 201-220, 221-240, 241-260, 261-280, 281-300, 301-320, 321-340, 341-360, 361-380, 381-400, 401-420, 421-440, 441-460, 461-480, 481-500, 501-520, 521-540, 541-560, 561-580, 581-600, 601-620, 621-640, 641-660, 661-680, 681-700, 701-720, 721-740, 741-760, 761-780, 781-800, 801-820, 821-840, 841-860, 861-880, 881-900, 901-920, 921-940, 941-960, 961-980, 981-1000, 1001-1020, 1021-1040, 1041-1060, 1061-1080, 1081-1100, 1101-1120, 1121-1140, 1141-1160, 1161-1180, 1181-1200, 1201-1220, 1221-1240, 1241-1260, 1261-1280, 1281-1300, 1301-1320, 1321-1340, 1341-1360, 1361-1380, 1381-1400, 1401-1420, 1421-1440, or 1441 to the end of the coding region of SEQ ID NO:Y. Moreover, polypeptide fragments of the invention may be at least about 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 100, 110, 120, 130, 140, or 150 amino acids in length. In this context “about” includes the particularly recited ranges or values, or ranges or values larger or smaller by several (5, 4, 3, 2, or 1) amino acids, at either extreme or at both extremes. Polynucleotides encoding these polypeptide fragments are also encompassed by the invention.

Even if deletion of one or more amino acids from the N-terminus of a protein results in modification of loss of one or more biological functions of the protein, other functional activities (e.g., biological activities; such as, for example, activity useful in detecting, preventing, diagnosing, prognosticating, treating, and/or ameliorating cancer and other hyperproliferative diseases and disorders; ability to multimerize; ability to bind a ligand; antigenic ability useful for production of polypeptide specific antibodies) may still be retained. For example, the ability of shortened muteins to induce and/or bind to antibodies which recognize the complete or mature forms of the polypeptides generally will be retained when less than the majority of the residues of the complete or mature polypeptide are removed from the N-terminus. Whether a particular polypeptide lacking N-terminal residues of a complete polypeptide retains such immunologic activities can readily be determined by routine methods described herein and otherwise known in the art. It is not unlikely that a mutein with a large number of deleted N-terminal amino acid residues may retain some biological or immunogenic activities. In fact, peptides composed of as few as six amino acid residues may often evoke an immune response.

Accordingly, polypeptide fragments include the secreted protein as well as the mature form. Further preferred polypeptide fragments include the secreted protein or the mature form having a continuous series of deleted residues from the amino or the carboxy terminus, or both. For example, any number of amino acids, ranging from 1-60, can be deleted from the amino terminus of either the secreted polypeptide or the mature form. Similarly, any number of amino acids, ranging from 1-30, can be deleted from the carboxy terminus of the secreted protein or mature form. Furthermore, any combination of the above amino and carboxy terminus deletions are preferred. Similarly, polynucleotides encoding these polypeptide fragments are also preferred.

The present invention further provides polypeptides having one or more residues deleted from the amino terminus of the amino acid sequence of a polypeptide disclosed herein (e.g., a polypeptide of SEQ ID NO:Y, a polypeptide as defined in columns 14 and 15 of Table 1A, a polypeptide encoded by the polynucleotide sequence contained in SEQ ID NO:X or the complement thereof, a polypeptide encoded by the portion of SEQ ID NO:X as defined in columns 8 and 9 of Table 2, a polypeptide encoded by the portion of SEQ ID NO:B as defined in column 6 of Table 1C, a polypeptide encoded by the cDNA contained in ATCC™ Deposit No:Z, and/or a mature polypeptide encoded by the cDNA contained in ATCC™ Deposit No:Z). In particular, N-terminal deletions may be described by the general formula m-q, where q is a whole integer representing the total number of amino acid residues in a polypeptide of the invention (e.g., the polypeptide disclosed in SEQ ID NO:Y, the mature (secreted) portion of SEQ ID NO:Y as defined in columns 14 and 15 of Table 1A, or the polypeptide encoded by the portion of SEQ ID NO:X as defined in columns 8 and 9 of Table 2), and m is defined as any integer ranging from 2 to q-6. Polynucleotides encoding these polypeptides are also encompassed by the invention.

The present invention further provides polypeptides having one or more residues from the carboxy terminus of the amino acid sequence of a polypeptide disclosed herein (e.g., a polypeptide of SEQ ID NO:Y, the mature (secreted) portion of SEQ ID NO:Y as defined in columns 14 and 15 of Table 1A, a polypeptide encoded by the polynucleotide sequence contained in SEQ ID NO:X, a polypeptide encoded by the portion of SEQ ID NO:X as defined in columns 8 and 9 of Table 2, a polypeptide encoded by the portion of SEQ ID NO:B as defined in column 6 of Table 1C, a polypeptide encoded by the cDNA contained in ATCC™ Deposit No:Z, and/or a mature polypeptide encoded by the cDNA contained in ATCC™ Deposit No:Z). In particular, C-terminal deletions may be described by the general formula 1-n, where n is any whole integer ranging from 6 to q-1, and where n corresponds to the position of amino acid residue in a polypeptide of the invention. Polynucleotides encoding these polypeptides are also encompassed by the invention.

In addition, any of the above described N- or C-terminal deletions can be combined to produce a N- and C-terminal deleted polypeptide. The invention also provides polypeptides having one or more amino acids deleted from both the amino and the carboxyl termini, which may be described generally as having residues m-n of a polypeptide encoded by SEQ ID NO:X (e.g., including, but not limited to, the preferred polypeptide disclosed as SEQ ID NO:Y, the mature (secreted) portion of SEQ ID NO:Y as defined in columns 14 and 15 of Table 1A, and the polypeptide encoded by the portion of SEQ ID NO:X as defined in columns 8 and 9 of Table 2), the cDNA contained in ATCC™ Deposit No:Z, and/or the complement thereof, where n and m are integers as described above. Polynucleotides encoding these polypeptides are also encompassed by the invention.

Also as mentioned above, even if deletion of one or more amino acids from the C-terminus of a protein results in modification of loss of one or more biological functions of the protein, other functional activities (e.g., biological activities such as, for example, activity useful in detecting, preventing, diagnosing, prognosticating, treating, and/or ameliorating cancer and other hyperproliferative diseases and disorders; ability to multimerize; ability to bind a ligand; antigenic ability useful for production of polypeptide specific antibodies) may still be retained. For example the ability of the shortened mutein to induce and/or bind to antibodies which recognize the complete or mature forms of the polypeptide generally will be retained when less than the majority of the residues of the complete or mature polypeptide are removed from the C-terminus. Whether a particular polypeptide lacking C-terminal residues of a complete polypeptide retains such immunologic activities can readily be determined by routine methods described herein and otherwise known in the art. It is not unlikely that a mutein with a large number of deleted C-terminal amino acid residues may retain some biological or immunogenic activities. In fact, peptides composed of as few as six amino acid residues may often evoke an immune response.

The present application is also directed to proteins containing polypeptides at least 80%, 85%, 90%, 95%, 96%, 97%, 98% or 99% identical to a polypeptide sequence set forth herein. In preferred embodiments, the application is directed to proteins containing polypeptides at least 80%, 85%, 90%, 95%, 96%, 97%, 98% or 99% identical to polypeptides having the amino acid sequence of the specific N- and C-terminal deletions. Polynucleotides encoding these polypeptides are also encompassed by the invention.

Any polypeptide sequence encoded by, for example, the polynucleotide sequences set forth as SEQ ID NO:X or the complement thereof, (presented, for example, in Tables 1A and 2), the cDNA contained in ATCC™ Deposit No:Z, or the polynucleotide sequence as defined in column 6 of Table 1C, may be analyzed to determine certain preferred regions of the polypeptide. For example, the amino acid sequence of a polypeptide encoded by a polynucleotide sequence of SEQ ID NO:X (e.g., the polypeptide of SEQ ID NO:Y and the polypeptide encoded by the portion of SEQ ID NO:X as defined in columns 8 and 9 of Table 2) or the cDNA contained in ATCC™ Deposit No:Z may be analyzed using the default parameters of the DNASTAR computer algorithm (DNASTAR, Inc., 1228 S. Park St., Madison, Wis. 53715 USA; http://www.dnastar.com/).

Polypeptide regions that may be routinely obtained using the DNASTAR computer algorithm include, but are not limited to, Garnier-Robson alpha-regions, beta-regions, turn-regions, and coil-regions; Chou-Fasman alpha-regions, beta-regions, and turn-regions; Kyte-Doolittle hydrophilic regions and hydrophobic regions; Eisenberg alpha- and beta-amphipathic regions; Karplus-Schulz flexible regions; Emini surface-forming regions; and Jameson-Wolf regions of high antigenic index. Among highly preferred polynucleotides of the invention in this regard are those that encode polypeptides comprising regions that combine several structural features, such as several (e.g., 1, 2, 3 or 4) of the features set out above.

Additionally, Kyte-Doolittle hydrophilic regions and hydrophobic regions, Emini surface-forming regions, and Jameson-Wolf regions of high antigenic index (i.e., containing four or more contiguous amino acids having an antigenic index of greater than or equal to 1.5, as identified using the default parameters of the Jameson-Wolf program) can routinely be used to determine polypeptide regions that exhibit a high degree of potential for antigenicity. Regions of high antigenicity are determined from data by DNASTAR analysis by choosing values which represent regions of the polypeptide which are likely to be exposed on the surface of the polypeptide in an environment in which antigen recognition may occur in the process of initiation of an immune response.

Preferred polypeptide fragments of the invention are fragments comprising, or alternatively, consisting of, an amino acid sequence that displays a functional activity (e.g. biological activity such as, for example, activity useful in detecting, preventing, diagnosing, prognosticating, treating, and/or ameliorating cancer and other hyperproliferative diseases and disorders; ability to multimerize; ability to bind a ligand; antigenic ability useful for production of polypeptide specific antibodies) of the polypeptide sequence of which the amino acid sequence is a fragment. By a polypeptide displaying a “functional activity” is meant a polypeptide capable of one or more known functional activities associated with a full-length protein, such as, for example, biological activity, antigenicity, immunogenicity, and/or multimerization, as described herein.

Other preferred polypeptide fragments are biologically active fragments. Biologically active fragments are those exhibiting activity similar, but not necessarily identical, to an activity of the polypeptide of the present invention. The biological activity of the fragments may include an improved desired activity, or a decreased undesirable activity.

In preferred embodiments, polypeptides of the invention comprise, or alternatively consist of, one, two, three, four, five or more of the antigenic fragments of the polypeptide of SEQ ID NO:Y, or portions thereof. Polynucleotides encoding these polypeptides are also encompassed by the invention.

Epitopes and Antibodies

The present invention encompasses polypeptides comprising, or alternatively consisting of, an epitope of: the polypeptide sequence shown in SEQ ID NO:Y; a polypeptide sequence encoded by SEQ ID NO:X or the complementary strand thereto; the polypeptide sequence encoded by the portion of SEQ ID NO:X as defined in columns 8 and 9 of Table 2; the polypeptide sequence encoded by the portion of SEQ ID NO:B as defined in column 6 of Table 1C or the complement thereto; the polypeptide sequence encoded by the cDNA contained in ATCC™ Deposit No:Z; or the polypeptide sequence encoded by a polynucleotide that hybridizes to the sequence of SEQ ID NO:X, the complement of the sequence of SEQ ID NO:X, the complement of a portion of SEQ ID NO:X as defined in columns 8 and 9 of Table 2, or the cDNA sequence contained in ATCC™ Deposit No:Z under stringent hybridization conditions or alternatively, under lower stringency hybridization as defined supra. The present invention further encompasses polynucleotide sequences encoding an epitope of a polypeptide sequence of the invention (such as, for example, the sequence disclosed in SEQ ID NO:X, or a fragment thereof), polynucleotide sequences of the complementary strand of a polynucleotide sequence encoding an epitope of the invention, and polynucleotide sequences which hybridize to the complementary strand under stringent hybridization conditions or alternatively, under lower stringency hybridization conditions defined supra.

The term “epitopes,” as used herein, refers to portions of a polypeptide having antigenic or immunogenic activity in an animal, preferably a mammal, and most preferably in a human. In a preferred embodiment, the present invention encompasses a polypeptide comprising an epitope, as well as the polynucleotide encoding this polypeptide. An “immunogenic epitope,” as used herein, is defined as a portion of a protein that elicits an antibody response in an animal, as determined by any method known in the art, for example, by the methods for generating antibodies described infra. (See, for example, Geysen et al., Proc. Natl. Acad. Sci. USA 81:3998-4002 (1983)). The term “antigenic epitope,” as used herein, is defined as a portion of a protein to which an antibody can immunospecifically bind its antigen as determined by any method well known in the art, for example, by the immunoassays described herein. Immunospecific binding excludes non-specific binding but does not necessarily exclude cross-reactivity with other antigens. Antigenic epitopes need not necessarily be immunogenic.

Fragments which function as epitopes may be produced by any conventional means. (See, e.g., Houghten, R. A., Proc. Natl. Acad. Sci. USA 82:5131-5135 (1985) further described in U.S. Pat. No. 4,631,211.)

In the present invention, antigenic epitopes preferably contain a sequence of at least 4, at least 5, at least 6, at least 7, more preferably at least 8, at least 9, at least 10, at least 11, at least 12, at least 13, at least 14, at least 15, at least 20, at least 25, at least 30, at least 40, at least 50, and, most preferably, between about 15 to about 30 amino acids. Preferred polypeptides comprising immunogenic or antigenic epitopes are at least 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, or 100 amino acid residues in length. Additional non-exclusive preferred antigenic epitopes include the antigenic epitopes disclosed herein, as well as portions thereof. Antigenic epitopes are useful, for example, to raise antibodies, including monoclonal antibodies, that specifically bind the epitope. Preferred antigenic epitopes include the antigenic epitopes disclosed herein, as well as any combination of two, three, four, five or more of these antigenic epitopes. Antigenic epitopes can be used as the target molecules in immunoassays. (See, for instance, Wilson et al., Cell 37:767-778 (1984); Sutcliffe et al., Science 219:660-666 (1983)).

Non-limiting examples of epitopes of polypeptides that can be used to generate antibodies of the invention include a polypeptide comprising, or alternatively consisting of, at least one, two, three, four, five, six or more of the portion(s) of SEQ ID NO:Y specified in column 6 of Table 1B.1. These polypeptide fragments have been determined to bear antigenic epitopes of the proteins of the invention by the analysis of the Jameson-Wolf antigenic index which is included in the DNAStar suite of computer programs. By “comprise” it is intended that a polypeptide contains at least one, two, three, four, five, six or more of the portion(s) of SEQ ID NO:Y shown in column 6 of Table 1B.1, but it may contain additional flanking residues on either the amino or carboxyl termini of the recited portion. Such additional flanking sequences are preferably sequences naturally found adjacent to the portion; i.e., contiguous sequence shown in SEQ ID NO:Y. The flanking sequence may, however, be sequences from a heterologous polypeptide, such as from another protein described herein or from a heterologous polypeptide not described herein. In particular embodiments, epitope portions of a polypeptide of the invention comprise one, two, three, or more of the portions of SEQ ID NO:Y shown in column 6 of Table Similarly, immunogenic epitopes can be used, for example, to induce antibodies according to methods well known in the art. See, for instance, Sutcliffe et al., supra; Wilson et al., supra; Chow et al., Proc. Natl. Acad. Sci. USA 82:910-914; and Bittle et al., J. Gen. Virol. 66:2347-2354 (1985). Preferred immunogenic epitopes include the immunogenic epitopes disclosed herein, as well as any combination of two, three, four, five or more of these immunogenic epitopes. The polypeptides comprising one or more immunogenic epitopes may be presented for eliciting an antibody response together with a carrier protein, such as an albumin, to an animal system (such as rabbit or mouse), or, if the polypeptide is of sufficient length (at least about 25 amino acids), the polypeptide may be presented without a carrier. However, immunogenic epitopes comprising as few as 8 to 10 amino acids have been shown to be sufficient to raise antibodies capable of binding to, at the very least, linear epitopes in a denatured polypeptide (e.g., in Western blotting).

Epitope-bearing polypeptides of the present invention may be used to induce antibodies according to methods well known in the art including, but not limited to, in vivo immunization, in vitro immunization, and phage display methods. See, e.g., Sutcliffe et al., supra; Wilson et al., supra, and Bittle et al., J. Gen. Virol., 66:2347-2354 (1985). If in vivo immunization is used, animals may be immunized with free peptide; however, anti-peptide antibody titer may be boosted by coupling the peptide to a macromolecular carrier, such as keyhole limpet hemacyanin (KLH) or tetanus toxoid. For instance, peptides containing cysteine residues may be coupled to a carrier using a linker such as maleimidobenzoyl-N-hydroxysuccinimide ester (MBS), while other peptides may be coupled to carriers using a more general linking agent such as glutaraldehyde. Animals such as rabbits, rats and mice are immunized with either free or carrier-coupled peptides, for instance, by intraperitoneal and/or intradermal injection of emulsions containing about 100 μg of peptide or carrier protein and Freund's adjuvant or any other adjuvant known for stimulating an immune response. Several booster injections may be needed, for instance, at intervals of about two weeks, to provide a useful titer of anti-peptide antibody which can be detected, for example, by ELISA assay using free peptide adsorbed to a solid surface. The titer of anti-peptide antibodies in serum from an immunized animal may be increased by selection of anti-peptide antibodies, for instance, by adsorption to the peptide on a solid support and elution of the selected antibodies according to methods well known in the art.

As one of skill in the art will appreciate, and as discussed above, the polypeptides of the present invention (e.g., those comprising an immunogenic or antigenic epitope) can be fused to heterologous polypeptide sequences. For example, polypeptides of the present invention (including fragments or variants thereof), may be fused with the constant domain of immunoglobulins (IgA, IgE, IgG, IgM), or portions thereof (CH1, CH2, CH3, or any combination thereof and portions thereof, resulting in chimeric polypeptides. By way of another non-limiting example, polypeptides and/or antibodies of the present invention (including fragments or variants thereof) may be fused with albumin (including but not limited to recombinant human serum albumin or fragments or variants thereof (see, e.g., U.S. Pat. No. 5,876,969, issued Mar. 2, 1999, EP Patent 0 413 622, and U.S. Pat. No. 5,766,883, issued Jun. 16, 1998, herein incorporated by reference in their entirety)). In a preferred embodiment, polypeptides and/or antibodies of the present invention (including fragments or variants thereof) are fused with the mature form of human serum albumin (i.e., amino acids 1-585 of human serum albumin as shown in FIGS. 1 and 2 of EP Patent 0 322 094) which is herein incorporated by reference in its entirety. In another preferred embodiment, polypeptides and/or antibodies of the present invention (including fragments or variants thereof) are fused with polypeptide fragments comprising, or alternatively consisting of, amino acid residues 1-z of human serum albumin, where z is an integer from 369 to 419, as described in U.S. Pat. No. 5,766,883 herein incorporated by reference in its entirety. Polypeptides and/or antibodies of the present invention (including fragments or variants thereof) may be fused to either the N- or C-terminal end of the heterologous protein (e.g., immunoglobulin Fc polypeptide or human serum albumin polypeptide). Polynucleotides encoding fusion proteins of the invention are also encompassed by the invention.

Such fusion proteins as those described above may facilitate purification and may increase half-life in vivo. This has been shown for chimeric proteins consisting of the first two domains of the human CD4-polypeptide and various domains of the constant regions of the heavy or light chains of mammalian immunoglobulins. See, e.g., EP 394,827; Traunecker et al., Nature, 331:84-86 (1988). Enhanced delivery of an antigen across the epithelial barrier to the immune system has been demonstrated for antigens (e.g., insulin) conjugated to an FcRn binding partner such as IgG or Fc fragments (see, e.g., PCT Publications WO 96/22024 and WO 99/04813). IgG fusion proteins that have a disulfide-linked dimeric structure due to the IgG portion desulfide bonds have also been found to be more efficient in binding and neutralizing other molecules than monomeric polypeptides or fragments thereof alone. See, e.g., Fountoulakis et al., J. Biochem., 270:3958-3964 (1995). Nucleic acids encoding the above epitopes can also be recombined with a gene of interest as an epitope tag (e.g., the hemagglutinin (HA) tag or flag tag) to aid in detection and purification of the expressed polypeptide. For example, a system described by Janknecht et al. allows for the ready purification of non-denatured fusion proteins expressed in human cell lines (Janknecht et al., 1991, Proc. Natl. Acad. Sci. USA 88:8972-897). In this system, the gene of interest is subcloned into a vaccinia recombination plasmid such that the open reading frame of the gene is translationally fused to an amino-terminal tag consisting of six histidine residues. The tag serves as a matrix binding domain for the fusion protein. Extracts from cells infected with the recombinant vaccinia virus are loaded onto Ni2+ nitriloacetic acid-agarose column and histidine-tagged proteins can be selectively eluted with imidazole-containing buffers.

Fusion Proteins

Any polypeptide of the present invention can be used to generate fusion proteins. For example, the polypeptide of the present invention, when fused to a second protein, can be used as an antigenic tag. Antibodies raised against the polypeptide of the present invention can be used to indirectly detect the second protein by binding to the polypeptide. Moreover, because secreted proteins target cellular locations based on trafficking signals, polypeptides of the present invention which are shown to be secreted can be used as targeting molecules once fused to other proteins.

Examples of domains that can be fused to polypeptides of the present invention include not only heterologous signal sequences, but also other heterologous functional regions. The fusion does not necessarily need to be direct, but may occur through linker sequences.

In certain preferred embodiments, proteins of the invention are fusion proteins comprising an amino acid sequence that is an N and/or C-terminal deletion of a polypeptide of the invention. In preferred embodiments, the invention is directed to a fusion protein comprising an amino acid sequence that is at least 90%, 95%, 96%, 97%, 98% or 99% identical to a polypeptide sequence of the invention. Polynucleotides encoding these proteins are also encompassed by the invention.

Moreover, fusion proteins may also be engineered to improve characteristics of the polypeptide of the present invention. For instance, a region of additional amino acids, particularly charged amino acids, may be added to the N-terminus of the polypeptide to improve stability and persistence during purification from the host cell or subsequent handling and storage. Also, peptide moieties may be added to the polypeptide to facilitate purification. Such regions may be removed prior to final preparation of the polypeptide. The addition of peptide moieties to facilitate handling of polypeptides are familiar and routine techniques in the art.

As one of skill in the art will appreciate that, as discussed above, polypeptides of the present invention, and epitope-bearing fragments thereof, can be combined with heterologous polypeptide sequences. For example, the polypeptides of the present invention may be fused with heterologous polypeptide sequences, for example, the polypeptides of the present invention may be fused with the constant domain of immunoglobulins (IgA, IgE, IgG, IgM) or portions thereof (CH1, CH2, CH3, and any combination thereof, including both entire domains and portions thereof), or albumin (including, but not limited to, native or recombinant human albumin or fragments or variants thereof (see, e.g., U.S. Pat. No. 5,876,969, issued Mar. 2, 1999, EP Patent 0 413 622, and U.S. Pat. No. 5,766,883, issued Jun. 16, 1998, herein incorporated by reference in their entirety)), resulting in chimeric polypeptides. For example, EP-A-O 464 533 (Canadian counterpart 2045869) discloses fusion proteins comprising various portions of constant region of immunoglobulin molecules together with another human protein or part thereof. In many cases, the Fc part in a fusion protein is beneficial in therapy and diagnosis, and thus can result in, for example, improved pharmacokinetic properties (EP-A 0232 262). Alternatively, deleting the Fc part after the fusion protein has been expressed, detected, and purified, would be desired. For example, the Fc portion may hinder therapy and diagnosis if the fusion protein is used as an antigen for immunizations. In drug discovery, for example, human proteins, such as hIL-5, have been fused with Fc portions for the purpose of high-throughput screening assays to identify antagonists of hIL-5. See, D. Bennett et al., J. Molecular Recognition 8:52-58 (1995); K. Johanson et al., J. Biol. Chem. 270:9459-9471 (1995).

Moreover, the polypeptides of the present invention can be fused to marker sequences, such as a polypeptide which facilitates purification of the fused polypeptide. In preferred embodiments, the marker amino acid sequence is a hexa-histidine peptide, such as the tag provided in a pQE vector (QIAGEN, Inc., 9259 Eton Avenue, Chatsworth, Calif., 91311), among others, many of which are commercially available. As described in Gentz et al., Proc. Natl. Acad. Sci. USA 86:821-824 (1989), for instance, hexa-histidine provides for convenient purification of the fusion protein. Another peptide tag useful for purification, the “HA” tag, corresponds to an epitope derived from the influenza hemagglutinin protein (Wilson et al., Cell 37:767 (1984)).

Additional fusion proteins of the invention may be generated through the techniques of gene-shuffling, motif-shuffling, exon-shuffling, and/or codon-shuffling (collectively referred to as “DNA shuffling”). DNA shuffling may be employed to modulate the activities of polypeptides of the invention, such methods can be used to generate polypeptides with altered activity, as well as agonists and antagonists of the polypeptides. See, generally, U.S. Pat. Nos. 5,605,793; 5,811,238; 5,830,721; 5,834,252; and 5,837,458, and Patten et al., Curr. Opinion Biotechnol. 8:724-33 (1997); Harayama, Trends Biotechnol. 16(2):76-82 (1998); Hansson, et al., J. Mol. Biol. 287:265-76 (1999); and Lorenzo and Blasco, Biotechniques 24(2):308-13 (1998) (each of these patents and publications are hereby incorporated by reference in its entirety). In one embodiment, alteration of polynucleotides corresponding to SEQ ID NO:X and the polypeptides encoded by these polynucleotides may be achieved by DNA shuffling. DNA shuffling involves the assembly of two or more DNA segments by homologous or site-specific recombination to generate variation in the polynucleotide sequence. In another embodiment, polynucleotides of the invention, or the encoded polypeptides, may be altered by being subjected to random mutagenesis by error-prone PCR, random nucleotide insertion or other methods prior to recombination. In another embodiment, one or more components, motifs, sections, parts, domains, fragments, etc., of a polynucleotide encoding a polypeptide of the invention may be recombined with one or more components, motifs, sections, parts, domains, fragments, etc. of one or more heterologous molecules.

Thus, any of these above fusions can be engineered using the polynucleotides or the polypeptides of the present invention.

Recombinant and Synthetic Production of Polypeptides of the Invention

The present invention also relates to vectors containing the polynucleotide of the present invention, host cells, and the production of polypeptides by synthetic and recombinant techniques. The vector may be, for example, a phage, plasmid, viral, or retroviral vector. Retroviral vectors may be replication competent or replication defective. In the latter case, viral propagation generally will occur only in complementing host cells.

The polynucleotides of the invention may be joined to a vector containing a selectable marker for propagation in a host. Generally, a plasmid vector is introduced in a precipitate, such as a calcium phosphate precipitate, or in a complex with a charged lipid. If the vector is a virus, it may be packaged in vitro using an appropriate packaging cell line and then transduced into host cells.

The polynucleotide insert should be operatively linked to an appropriate promoter, such as the phage lambda PL promoter, the E. coli lac, trp, phoA and tac promoters, the SV40 early and late promoters and promoters of retroviral LTRs, to name a few. Other suitable promoters will be known to the skilled artisan. The expression constructs will further contain sites for transcription initiation, termination, and, in the transcribed region, a ribosome binding site for translation. The coding portion of the transcripts expressed by the constructs will preferably include a translation initiating codon at the beginning and a termination codon (UAA, UGA or UAG) appropriately positioned at the end of the polypeptide to be translated.

As indicated, the expression vectors will preferably include at least one selectable marker. Such markers include dihydrofolate reductase, G418, glutamine synthase, or neomycin resistance for eukaryotic cell culture, and tetracycline, kanamycin or ampicillin resistance genes for culturing in E. coli and other bacteria. Representative examples of appropriate hosts include, but are not limited to, bacterial cells, such as E. coli, Streptomyces and Salmonella typhimurium cells; fungal cells, such as yeast cells (e.g., Saccharomyces cerevisiae or Pichia pastoris (ATCC™ Accession No. 201178)); insect cells such as Drosophila S2 and Spodoptera Sf9 cells; animal cells such as CHO, COS, 293, and Bowes melanoma cells; and plant cells. Appropriate culture mediums and conditions for the above-described host cells are known in the art.

Among vectors preferred for use in bacteria include pQE70, pQE60 and pQE-9, available from QIAGEN, Inc.; pBLUESCRIPT™ vectors, Phagescript vectors, pNH8A, pNH16a, pNH18A, pNH46A, available from STRATAGENE™ Cloning Systems, Inc.; and ptrc99a, pKK223-3, pKK233-3, pDR540, pRIT5 available from PHARMACIA™ Biotech, Inc. Among preferred eukaryotic vectors are pWLNEO, pSV2CAT, pOG44, pXT1 and pSG available from STRATAGENE™; and pSVK3, pBPV, pMSG and pSVL available from PHARMACIA™. Preferred expression vectors for use in yeast systems include, but are not limited to pYES2, pYD1, pTEF1/Zeo, pYES2/GS, pPICZ, pGAPZ, pGAPZalph, pPIC9, pPIC3.5, pHIL-D2, pHIL-S1, pPIC3.5K, pPIC9K, and PA0815 (all available from Invitrogen, Carlbad, Calif.). Other suitable vectors will be readily apparent to the skilled artisan.

Vectors which use glutamine synthase (GS) or DHFR as the selectable markers can be amplified in the presence of the drugs methionine sulphoximine or methotrexate, respectively. An advantage of glutamine synthase based vectors are the availabilty of cell lines (e.g., the murine myeloma cell line, NS0) which are glutamine synthase negative. Glutamine synthase expression systems can also function in glutamine synthase expressing cells (e.g., Chinese Hamster Ovary (CHO) cells) by providing additional inhibitor to prevent the functioning of the endogenous gene. A glutamine synthase expression system and components thereof are detailed in PCT publications: WO87/04462; WO86/05807; WO89/01036; WO89/10404; and WO91/06657, which are hereby incorporated in their entireties by reference herein. Additionally, glutamine synthase expression vectors can be obtained from Lonza Biologics, Inc. (Portsmouth, N.H.). Expression and production of monoclonal antibodies using a GS expression system in murine myeloma cells is described in Bebbington et al., Bio/technology 10:169 (1992) and in Biblia and Robinson Biotechnot. Prog. 11: 1 (1995) which are herein incorporated by reference.

The present invention also relates to host cells containing the above-described vector constructs described herein, and additionally encompasses host cells containing nucleotide sequences of the invention that are operably associated with one or more heterologous control regions (e.g., promoter and/or enhancer) using techniques known of in the art. The host cell can be a higher eukaryotic cell, such as a mammalian cell (e.g., a human derived cell), or a lower eukaryotic cell, such as a yeast cell, or the host cell can be a prokaryotic cell, such as a bacterial cell. A host strain may be chosen which modulates the expression of the inserted gene sequences, or modifies and processes the gene product in the specific fashion desired. Expression from certain promoters can be elevated in the presence of certain inducers; thus expression of the genetically engineered polypeptide may be controlled. Furthermore, different host cells have characteristics and specific mechanisms for the translational and post-translational processing and modification (e.g., phosphorylation, cleavage) of proteins. Appropriate cell lines can be chosen to ensure the desired modifications and processing of the foreign protein expressed.

Introduction of the nucleic acids and nucleic acid constructs of the invention into the host cell can be effected by calcium phosphate transfection, DEAE-dextran mediated transfection, cationic lipid-mediated transfection, electroporation, transduction, infection, or other methods. Such methods are described in many standard laboratory manuals, such as Davis et al., Basic Methods In Molecular Biology (1986). It is specifically contemplated that the polypeptides of the present invention may in fact be expressed by a host cell lacking a recombinant vector.

In addition to encompassing host cells containing the vector constructs discussed herein, the invention also encompasses primary, secondary, and immortalized host cells of vertebrate origin, particularly mammalian origin, that have been engineered to delete or replace endogenous genetic material (e.g., the coding sequence), and/or to include genetic material (e.g., heterologous polynucleotide sequences) that is operably associated with polynucleotides of the invention, and which activates, alters, and/or amplifies endogenous polynucleotides. For example, techniques known in the art may be used to operably associate heterologous control regions (e.g., promoter and/or enhancer) and endogenous polynucleotide sequences via homologous recombination (see, e.g., U.S. Pat. No. 5,641,670, issued Jun. 24, 1997; International Publication Number WO 96/29411; International Publication Number WO 94/12650; Koller et al., Proc. Natl. Acad. Sci. USA 86:8932-8935 (1989); and Zijlstra et al., Nature 342:435-438 (1989), the disclosures of each of which are incorporated by reference in their entireties).

Polypeptides of the invention can be recovered and purified from recombinant cell cultures by well-known methods including ammonium sulfate or ethanol precipitation, acid extraction, anion or cation exchange chromatography, phosphocellulose chromatography, hydrophobic interaction chromatography, affinity chromatography, hydroxylapatite chromatography and lectin chromatography. Most preferably, high performance liquid chromatography (“HPLC”) is employed for purification.

Polypeptides of the present invention can also be recovered from: products purified from natural sources, including bodily fluids, tissues and cells, whether directly isolated or cultured; products of chemical synthetic procedures; and products produced by recombinant techniques from a prokaryotic or eukaryotic host, including, for example, bacterial, yeast, higher plant, insect, and mammalian cells. Depending upon the host employed in a recombinant production procedure, the polypeptides of the present invention may be glycosylated or may be non-glycosylated. In addition, polypeptides of the invention may also include an initial modified methionine residue, in some cases as a result of host-mediated processes. Thus, it is well known in the art that the N-terminal methionine encoded by the translation initiation codon generally is removed with high efficiency from any protein after translation in all eukaryotic cells. While the N-terminal methionine on most proteins also is efficiently removed in most prokaryotes, for some proteins, this prokaryotic removal process is inefficient, depending on the nature of the amino acid to which the N-terminal methionine is covalently linked.

In one embodiment, the yeast Pichia pastoris is used to express polypeptides of the invention in a eukaryotic system. Pichia pastoris is a methylotrophic yeast which can metabolize methanol as its sole carbon source. A main step in the methanol metabolization pathway is the oxidation of methanol to formaldehyde using O₂. This reaction is catalyzed by the enzyme alcohol oxidase. In order to metabolize methanol as its sole carbon source, Pichia pastoris must generate high levels of alcohol oxidase due, in part, to the relatively low affinity of alcohol oxidase for O₂. Consequently, in a growth medium depending on methanol as a main carbon source, the promoter region of one of the two alcohol oxidase genes (AOX1) is highly active. In the presence of methanol, alcohol oxidase produced from the AOX1 gene comprises up to approximately 30% of the total soluble protein in Pichia pastoris. See Ellis, S. B., et al, Mol Cell Biol. 5:1111-21 (1985); Koutz, P. J, et al., Yeast 5:167-77 (1989); Tschopp, J. F., et al., Nucl. Acids Res. 15:3859-76 (1987). Thus, a heterologous coding sequence, such as, for example, a polynucleotide of the present invention, under the transcriptional regulation of all or part of the AOX1 regulatory sequence is expressed at exceptionally high levels in Pichia yeast grown in the presence of methanol.

In one example, the plasmid vector pPIC9K is used to express DNA encoding a polypeptide of the invention, as set forth herein, in a Pichea yeast system essentially as described in “Pichia Protocols: Methods in Molecular Biology,” D. R. Higgins and J. Cregg, eds. The Humana Press, Totowa, N.J., 1998. This expression vector allows expression and secretion of a polypeptide of the invention by virtue of the strong AOX1 promoter linked to the Pichia pastoris alkaline phosphatase (PHO) secretory signal peptide (i.e., leader) located upstream of a multiple cloning site.

Many other yeast vectors could be used in place of pPIC9K, such as, pYES2, pYD1, pTEF1/Zeo, pYES2/GS, pPICZ, pGAPZ, pGAPZalpha, pPIC9, pPIC3.5, pHIL-D2, pHIL-SI, pPIC3.5K, and PAO815, as one skilled in the art would readily appreciate, as long as the proposed expression construct provides appropriately located signals for transcription, translation, secretion (if desired), and the like, including an in-frame AUG as required.

In another embodiment, high-level expression of a heterologous coding sequence, such as, for example, a polynucleotide of the present invention, may be achieved by cloning the heterologous polynucleotide of the invention into an expression vector such as, for example, pGAPZ or pGAPZalpha, and growing the yeast culture in the absence of methanol.

In addition to encompassing host cells containing the vector constructs discussed herein, the invention also encompasses primary, secondary, and immortalized host cells of vertebrate origin, particularly mammalian origin, that have been engineered to delete or replace endogenous genetic material (e.g., coding sequence), and/or to include genetic material (e.g., heterologous polynucleotide sequences) that is operably associated with polynucleotides of the invention, and which activates, alters, and/or amplifies endogenous polynucleotides. For example, techniques known in the art may be used to operably associate heterologous control regions (e.g., promoter and/or enhancer) and endogenous polynucleotide sequences via homologous recombination (see, e.g., U.S. Pat. No. 5,641,670, issued Jun. 24, 1997; International Publication No. WO 96/29411, published Sep. 26, 1996; International Publication No. WO 94/12650, published Aug. 4, 1994; Koller et al., Proc. Natl. Acad. Sci. USA 86:8932-8935 (1989); and Zijlstra et al., Nature 342:435-438 (1989), the disclosures of each of which are incorporated by reference in their entireties).

In addition, polypeptides of the invention can be chemically synthesized using techniques known in the art (e.g., see Creighton, 1983, Proteins: Structures and Molecular Principles, W.H. Freeman & Co., N.Y., and Hunkapiller et al., Nature, 310:105-111 (1984)). For example, a polypeptide corresponding to a fragment of a polypeptide can be synthesized by use of a peptide synthesizer. Furthermore, if desired, nonclassical amino acids or chemical amino acid analogs can be introduced as a substitution or addition into the polypeptide sequence. Non-classical amino acids include, but are not limited to, to the D-isomers of the common amino acids, 2,4-diaminobutyric acid, α-amino isobutyric acid, 4-aminobutyric acid, Abu, 2-amino butyric acid, g-Abu, e-Ahx, 6-amino hexanoic acid, Aib, 2-amino isobutyric acid, 3-amino propionic acid, ornithine, norleucine, norvaline, hydroxyproline, sarcosine, citrulline, homocitrulline, cysteic acid, t-butylglycine, t-butylalanine, phenylglycine, cyclohexylalanine, b-alanine, fluoro-amino acids, designer amino acids such as b-methyl amino acids, Ca-methyl amino acids, Na-methyl amino acids, and amino acid analogs in general. Furthermore, the amino acid can be D (dextrorotary) or L (levorotary).

The invention encompasses polypeptides of the present invention which are differentially modified during or after translation, e.g., by glycosylation, acetylation, phosphorylation, amidation, derivatization by known protecting/blocking groups, proteolytic cleavage, linkage to an antibody molecule or other cellular ligand, etc. Any of numerous chemical modifications may be carried out by known techniques, including but not limited, to specific chemical cleavage by cyanogen bromide, trypsin, chymotrypsin, papain, V8 protease, NaBH₄; acetylation, formylation, oxidation, reduction; metabolic synthesis in the presence of tunicamycin; etc.

Additional post-translational modifications encompassed by the invention include, for example, e.g., N-linked or O-linked carbohydrate chains, processing of N-terminal or C-terminal ends), attachment of chemical moieties to the amino acid backbone, chemical modifications of N-linked or O-linked carbohydrate chains, and addition or deletion of an N-terminal methionine residue as a result of procaryotic host cell expression. The polypeptides may also be modified with a detectable label, such as an enzymatic, fluorescent, isotopic or affinity label to allow for detection and isolation of the protein.

Examples of suitable enzymes include horseradish peroxidase, alkaline phosphatase, beta-galactosidase, or acetylcholinesterase; examples of suitable prosthetic group complexes include streptavidin/biotin and avidin/biotin; examples of suitable fluorescent materials include umbelliferone, fluorescein, fluorescein isothiocyanate, rhodamine, dichlorotriazinylamine fluorescein, dansyl chloride or phycoerythrin; an example of a luminescent material includes luminol; examples of bioluminescent materials include luciferase, luciferin, and aequorin; and examples of suitable radioactive material include iodine (¹²¹I, ¹²³I, ¹²⁵I, ¹³¹I), carbon (¹⁴C), sulfur (³⁵S), tritium (³H), indium (¹¹¹In, ¹¹²In, ^(113m)In, ^(115m)In), technetium (⁹⁹Tc, ^(99m)Tc), thallium (²⁰¹Ti), gallium (⁶⁸Ga, ⁶⁷Ga), palladium (¹⁰³Pd), molybdenum (⁹⁹Mo), xenon (¹³³Xe), fluorine (¹⁸F), ¹⁵³Sm, ¹⁷⁷Lu, ¹⁵⁹Gd, ¹⁴⁹Pm, ¹⁴⁰ La, ¹⁷⁵Yb, ¹⁶ Ho, ⁹⁰Y, ⁴⁷Sc, ¹⁸⁶Re, ¹⁸⁸Re, ¹⁴²Pr, ¹⁰⁵Rh, and ⁹⁷Ru.

In specific embodiments, a polypeptide of the present invention or fragment or variant thereof is attached to macrocyclic chelators that associate with radiometal ions, including but not limited to, ¹⁷⁷Lu, ⁹⁰Y, ¹⁶⁶Ho, and ¹⁵³Sm, to polypeptides. In a preferred embodiment, the radiometal ion associated with the macrocyclic chelators is ¹¹¹In. In another preferred embodiment, the radiometal ion associated with the macrocyclic chelator is ⁹⁰Y. In specific embodiments, the macrocyclic chelator is 1,4,7,10-tetraazacyclododecane-N,N′,N″,N′″-tetraacetic acid (DOTA). In other specific embodiments, DOTA is attached to an antibody of the invention or fragment thereof via a linker molecule. Examples of linker molecules useful for conjugating DOTA to a polypeptide are commonly known in the art—see, for example, DeNardo et al., Clin Cancer Res. 4(10):2483-90 (1998); Peterson et al., Bioconjug. Chem. 10(4):553-7 (1999); and Zimmerman et al., Nucl. Med. Biol. 26(8):943-50 (1999); which are hereby incorporated by reference in their entirety.

As mentioned, the proteins of the invention may be modified by either natural processes, such as posttranslational processing, or by chemical modification techniques which are well known in the art. It will be appreciated that the same type of modification may be present in the same or varying degrees at several sites in a given polypeptide. Polypeptides of the invention may be branched, for example, as a result of ubiquitination, and they may be cyclic, with or without branching. Cyclic, branched, and branched cyclic polypeptides may result from posttranslation natural processes or may be made by synthetic methods. Modifications include acetylation, acylation, ADP-ribosylation, amidation, covalent attachment of flavin, covalent attachment of a heme moiety, covalent attachment of a nucleotide or nucleotide derivative, covalent attachment of a lipid or lipid derivative, covalent attachment of phosphotidylinositol, cross-linking, cyclization, disulfide bond formation, demethylation, formation of covalent cross-links, formation of cysteine, formation of pyroglutamate, formylation, gamma-carboxylation, glycosylation, GPI anchor formation, hydroxylation, iodination, methylation, myristoylation, oxidation, pegylation, proteolytic processing, phosphorylation, prenylation, racemization, selenoylation, sulfation, transfer-RNA mediated addition of amino acids to proteins such as arginylation, and ubiquitination. (See, for instance, PROTEINS—STRUCTURE AND MOLECULAR PROPERTIES, 2nd Ed., T. E. Creighton, W. H. Freeman and Company, New York (1993); POSTTRANSLATIONAL COVALENT MODIFICATION OF PROTEINS, B. C. Johnson, Ed., Academic Press, New York, pgs. 1-12 (1983); Seifter et al., Meth. Enzymol. 182:626-646 (1990); Rattan et al., Ann. N.Y. Acad. Sci. 663:48-62 (1992)).

Also provided by the invention are chemically modified derivatives of the polypeptides of the invention which may provide additional advantages such as increased solubility, stability and circulating time of the polypeptide, or decreased immunogenicity (see U.S. Pat. No. 4,179,337). The chemical moieties for derivitization may be selected from water soluble polymers such as polyethylene glycol, ethylene glycol/propylene glycol copolymers, carboxymethylcellulose, dextran, polyvinyl alcohol and the like. The polypeptides may be modified at random positions within the molecule, or at predetermined positions within the molecule and may include one, two, three or more attached chemical moieties.

The polymer may be of any molecular weight, and may be branched or unbranched. For polyethylene glycol, the preferred molecular weight is between about 1 kDa and about 100 kDa (the term “about” indicating that in preparations of polyethylene glycol, some molecules will weigh more, some less, than the stated molecular weight) for ease in handling and manufacturing. Other sizes may be used, depending on the desired therapeutic profile (e.g., the duration of sustained release desired, the effects, if any on biological activity, the ease in handling, the degree or lack of antigenicity and other known effects of the polyethylene glycol to a therapeutic protein or analog). For example, the polyethylene glycol may have an average molecular weight of about 200, 500, 1000, 1500, 2000, 2500, 3000, 3500, 4000, 4500, 5000, 5500, 6000, 6500, 7000, 7500, 8000, 8500, 9000, 9500, 10,000, 10,500, 11,000, 11,500, 12,000, 12,500, 13,000, 13,500, 14,000, 14,500, 15,000, 15,500, 16,000, 16,500, 17,000, 17,500, 18,000, 18,500, 19,000, 19,500, 20,000, 25,000, 30,000, 35,000, 40,000, 45,000, 50,000, 55,000, 60,000, 65,000, 70,000, 75,000, 80,000, 85,000, 90,000, 95,000, or 100,000 kDa.

As noted above, the polyethylene glycol may have a branched structure. Branched polyethylene glycols are described, for example, in U.S. Pat. No. 5,643,575; Morpurgo et al., Appl. Biochem. Biotechnol. 56:59-72 (1996); Vorobjev et al., Nucleosides Nucleotides 18:2745-2750 (1999); and Caliceti et al., Bioconjug. Chem. 10:638-646 (1999), the disclosures of each of which are incorporated herein by reference.

The polyethylene glycol molecules (or other chemical moieties) should be attached to the protein with consideration of effects on functional or antigenic domains of the protein. There are a number of attachment methods available to those skilled in the art, such as, for example, the method disclosed in EP 0 401 384 (coupling PEG to G-CSF), herein incorporated by reference; see also Malik et al., Exp. Hematol. 20:1028-1035 (1992), reporting pegylation of GM-CSF using tresyl chloride. For example, polyethylene glycol may be covalently bound through amino acid residues via a reactive group, such as a free amino or carboxyl group. Reactive groups are those to which an activated polyethylene glycol molecule may be bound. The amino acid residues having a free amino group may include lysine residues and the N-terminal amino acid residues; those having a free carboxyl group may include aspartic acid residues glutamic acid residues and the C-terminal amino acid residue. Sulfhydryl groups may also be used as a reactive group for attaching the polyethylene glycol molecules. Preferred for therapeutic purposes is attachment at an amino group, such as attachment at the N-terminus or lysine group.

As suggested above, polyethylene glycol may be attached to proteins via linkage to any of a number of amino acid residues. For example, polyethylene glycol can be linked to proteins via covalent bonds to lysine, histidine, aspartic acid, glutamic acid, or cysteine residues. One or more reaction chemistries may be employed to attach polyethylene glycol to specific amino acid residues (e.g., lysine, histidine, aspartic acid, glutamic acid, or cysteine) of the protein or to more than one type of amino acid residue (e.g., lysine, histidine, aspartic acid, glutamic acid, cysteine and combinations thereof) of the protein.

One may specifically desire proteins chemically modified at the N-terminus. Using polyethylene glycol as an illustration of the present composition, one may select from a variety of polyethylene glycol molecules (by molecular weight, branching, etc.), the proportion of polyethylene glycol molecules to protein (polypeptide) molecules in the reaction mix, the type of pegylation reaction to be performed, and the method of obtaining the selected N-terminally pegylated protein. The method of obtaining the N-terminally pegylated preparation (i.e., separating this moiety from other monopegylated moieties if necessary) may be by purification of the N-terminally pegylated material from a population of pegylated protein molecules. Selective proteins chemically modified at the N-terminus modification may be accomplished by reductive alkylation which exploits differential reactivity of different types of primary amino groups (lysine versus the N-terminal) available for derivatization in a particular protein. Under the appropriate reaction conditions, substantially selective derivatization of the protein at the N-terminus with a carbonyl group containing polymer is achieved.

As indicated above, pegylation of the proteins of the invention may be accomplished by any number of means. For example, polyethylene glycol may be attached to the protein either directly or by an intervening linker. Linkerless systems for attaching polyethylene glycol to proteins are described in Delgado et al., Crit. Rev. Thera. Drug Carrier Sys. 9:249-304 (1992); Francis et al., Intern. J. of Hematol. 68:1-18 (1998); U.S. Pat. No. 4,002,531; U.S. Pat. No. 5,349,052; WO 95/06058; and WO 98/32466, the disclosures of each of which are incorporated herein by reference.

One system for attaching polyethylene glycol directly to amino acid residues of proteins without an intervening linker employs tresylated MPEG, which is produced by the modification of monmethoxy polyethylene glycol (MPEG) using tresylchloride (ClSO₂CH₂CF₃)— Upon reaction of protein with tresylated MPEG, polyethylene glycol is directly attached to amine groups of the protein. Thus, the invention includes protein-polyethylene glycol conjugates produced by reacting proteins of the invention with a polyethylene glycol molecule having a 2,2,2-trifluoreothane sulphonyl group.

Polyethylene glycol can also be attached to proteins using a number of different intervening linkers. For example, U.S. Pat. No. 5,612,460, the entire disclosure of which is incorporated herein by reference, discloses urethane linkers for connecting polyethylene glycol to proteins. Protein-polyethylene glycol conjugates wherein the polyethylene glycol is attached to the protein by a linker can also be produced by reaction of proteins with compounds such as MPEG-succinimidylsuccinate, MPEG activated with 1,1′-carbonyldiimidazole, MPEG-2,4,5-trichloropenylcarbonate, MPEG-p-nitrophenolcarbonate, and various MPEG-succinate derivatives. A number of additional polyethylene glycol derivatives and reaction chemistries for attaching polyethylene glycol to proteins are described in International Publication No. WO 98/32466, the entire disclosure of which is incorporated herein by reference. Pegylated protein products produced using the reaction chemistries set out herein are included within the scope of the invention.

The number of polyethylene glycol moieties attached to each protein of the invention (i.e., the degree of substitution) may also vary. For example, the pegylated proteins of the invention may be linked, on average, to 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 12, 15, 17, 20, or more polyethylene glycol molecules. Similarly, the average degree of substitution within ranges such as 1-3, 2-4, 3-5, 4-6, 5-7, 6-8, 7-9, 8-10, 9-11, 10-12, 11-13, 12-14, 13-15, 14-16, 15-17, 16-18, 17-19, or 18-20 polyethylene glycol moieties per protein molecule. Methods for determining the degree of substitution are discussed, for example, in Delgado et al., Crit. Rev. Thera. Drug Carrier Sys. 9:249-304 (1992).

The polypeptides of the invention can be recovered and purified from chemical synthesis and recombinant cell cultures by standard methods which include, but are not limited to, ammonium sulfate or ethanol precipitation, acid extraction, anion or cation exchange chromatography, phosphocellulose chromatography, hydrophobic interaction chromatography, affinity chromatography, hydroxylapatite chromatography and lectin chromatography. Most preferably, high performance liquid chromatography (“HPLC”) is employed for purification. Well known techniques for refolding protein may be employed to regenerate active conformation when the polypeptide is denatured during isolation and/or purification.

The polypeptides of the invention may be in monomers or multimers (i.e., dimers, trimers, tetramers and higher multimers). Accordingly, the present invention relates to monomers and multimers of the polypeptides of the invention, their preparation, and compositions (preferably, Therapeutics) containing them. In specific embodiments, the polypeptides of the invention are monomers, dimers, trimers or tetramers. In additional embodiments, the multimers of the invention are at least dimers, at least trimers, or at least tetramers.

Multimers encompassed by the invention may be homomers or heteromers. As used herein, the term homomer refers to a multimer containing only polypeptides corresponding to a protein of the invention (e.g., the amino acid sequence of SEQ ID NO:Y, an amino acid sequence encoded by SEQ ID NO:X or the complement of SEQ ID NO:X, the amino acid sequence encoded by the portion of SEQ ID NO:X as defined in columns 8 and 9 of Table 2, and/or an amino acid sequence encoded by cDNA contained in ATCC™ Deposit No:Z (including fragments, variants, splice variants, and fusion proteins, corresponding to these as described herein)). These homomers may contain polypeptides having identical or different amino acid sequences. In a specific embodiment, a homomer of the invention is a multimer containing only polypeptides having an identical amino acid sequence. In another specific embodiment, a homomer of the invention is a multimer containing polypeptides having different amino acid sequences. In specific embodiments, the multimer of the invention is a homodimer (e.g., containing two polypeptides having identical or different amino acid sequences) or a homotrimer (e.g., containing three polypeptides having identical and/or different amino acid sequences). In additional embodiments, the homomeric multimer of the invention is at least a homodimer, at least a homotrimer, or at least a homotetramer.

As used herein, the term heteromer refers to a multimer containing one or more heterologous polypeptides (i.e., polypeptides of different proteins) in addition to the polypeptides of the invention. In a specific embodiment, the multimer of the invention is a heterodimer, a heterotrimer, or a heterotetramer. In additional embodiments, the heteromeric multimer of the invention is at least a heterodimer, at least a heterotrimer, or at least a heterotetramer.

Multimers of the invention may be the result of hydrophobic, hydrophilic, ionic and/or covalent associations and/or may be indirectly linked by, for example, liposome formation. Thus, in one embodiment, multimers of the invention, such as, for example, homodimers or homotrimers, are formed when polypeptides of the invention contact one another in solution. In another embodiment, heteromultimers of the invention, such as, for example, heterotrimers or heterotetramers, are formed when polypeptides of the invention contact antibodies to the polypeptides of the invention (including antibodies to the heterologous polypeptide sequence in a fusion protein of the invention) in solution. In other embodiments, multimers of the invention are formed by covalent associations with and/or between the polypeptides of the invention. Such covalent associations may involve one or more amino acid residues contained in the polypeptide sequence (e.g., that recited in SEQ ID NO:Y, encoded by the portion of SEQ ID NO:X as defined in columns 8 and 9 of Table 2, and/or encoded by the cDNA contained in ATCC™ Deposit No:Z). In one instance, the covalent associations are cross-linking between cysteine residues located within the polypeptide sequences which interact in the native (i.e., naturally occurring) polypeptide. In another instance, the covalent associations are the consequence of chemical or recombinant manipulation. Alternatively, such covalent associations may involve one or more amino acid residues contained in the heterologous polypeptide sequence in a fusion protein. In one example, covalent associations are between the heterologous sequence contained in a fusion protein of the invention (see, e.g., U.S. Pat. No. 5,478,925). In a specific example, the covalent associations are between the heterologous sequence contained in a Fc fusion protein of the invention (as described herein). In another specific example, covalent associations of fusion proteins of the invention are between heterologous polypeptide sequence from another protein that is capable of forming covalently associated multimers, such as for example, osteoprotegerin (see, e.g., International Publication NO: WO 98/49305, the contents of which are herein incorporated by reference in its entirety). In another embodiment, two or more polypeptides of the invention are joined through peptide linkers. Examples include those peptide linkers described in U.S. Pat. No. 5,073,627 (hereby incorporated by reference). Proteins comprising multiple polypeptides of the invention separated by peptide linkers may be produced using conventional recombinant DNA technology.

Another method for preparing multimer polypeptides of the invention involves use of polypeptides of the invention fused to a leucine zipper or isoleucine zipper polypeptide sequence. Leucine zipper and isoleucine zipper domains are polypeptides that promote multimerization of the proteins in which they are found. Leucine zippers were originally identified in several DNA-binding proteins (Landschulz et al., Science 240:1759, (1988)), and have since been found in a variety of different proteins. Among the known leucine zippers are naturally occurring peptides and derivatives thereof that dimerize or trimerize. Examples of leucine zipper domains suitable for producing soluble multimeric proteins of the invention are those described in PCT application WO 94/10308, hereby incorporated by reference. Recombinant fusion proteins comprising a polypeptide of the invention fused to a polypeptide sequence that dimerizes or trimerizes in solution are expressed in suitable host cells, and the resulting soluble multimeric fusion protein is recovered from the culture supernatant using techniques known in the art.

Trimeric polypeptides of the invention may offer the advantage of enhanced biological activity. Preferred leucine zipper moieties and isoleucine moieties are those that preferentially form trimers. One example is a leucine zipper derived from lung surfactant protein D (SPD), as described in Hoppe et al. (FEBS Letters 344:191, (1994)) and in U.S. patent application Ser. No. 08/446,922, hereby incorporated by reference. Other peptides derived from naturally occurring trimeric proteins may be employed in preparing trimeric polypeptides of the invention.

In another example, proteins of the invention are associated by interactions between Flag® polypeptide sequence contained in fusion proteins of the invention containing Flag® polypeptide sequence. In a further embodiment, proteins of the invention are associated by interactions between heterologous polypeptide sequence contained in Flag® fusion proteins of the invention and anti-Flag® antibody.

The multimers of the invention may be generated using chemical techniques known in the art. For example, polypeptides desired to be contained in the multimers of the invention may be chemically cross-linked using linker molecules and linker molecule length optimization techniques known in the art (see, e.g., U.S. Pat. No. 5,478,925, which is herein incorporated by reference in its entirety). Additionally, multimers of the invention may be generated using techniques known in the art to form one or more inter-molecule cross-links between the cysteine residues located within the sequence of the polypeptides desired to be contained in the multimer (see, e.g., U.S. Pat. No. 5,478,925, which is herein incorporated by reference in its entirety). Further, polypeptides of the invention may be routinely modified by the addition of cysteine or biotin to the C-terminus or N-terminus of the polypeptide and techniques known in the art may be applied to generate multimers containing one or more of these modified polypeptides (see, e.g., U.S. Pat. No. 5,478,925, which is herein incorporated by reference in its entirety). Additionally, techniques known in the art may be applied to generate liposomes containing the polypeptide components desired to be contained in the multimer of the invention (see, e.g., U.S. Pat. No. 5,478,925, which is herein incorporated by reference in its entirety).

Alternatively, multimers of the invention may be generated using genetic engineering techniques known in the art. In one embodiment, polypeptides contained in multimers of the invention are produced recombinantly using fusion protein technology described herein or otherwise known in the art (see, e.g., U.S. Pat. No. 5,478,925, which is herein incorporated by reference in its entirety). In a specific embodiment, polynucleotides coding for a homodimer of the invention are generated by ligating a polynucleotide sequence encoding a polypeptide of the invention to a sequence encoding a linker polypeptide and then further to a synthetic polynucleotide encoding the translated product of the polypeptide in the reverse orientation from the original C-terminus to the N-terminus (lacking the leader sequence) (see, e.g., U.S. Pat. No. 5,478,925, which is herein incorporated by reference in its entirety). In another embodiment, recombinant techniques described herein or otherwise known in the art are applied to generate recombinant polypeptides of the invention which contain a transmembrane domain (or hydrophobic or signal peptide) and which can be incorporated by membrane reconstitution techniques into liposomes (see, e.g., U.S. Pat. No. 5,478,925, which is herein incorporated by reference in its entirety).

Antibodies

Further polypeptides of the invention relate to antibodies and T-cell antigen receptors (TCR) which immunospecifically bind a polypeptide, polypeptide fragment, or variant of the invention (e.g., a polypeptide or fragment or variant of the amino acid sequence of SEQ ID NO:Y or a polypeptide encoded by the cDNA contained in ATCC™ Deposit No:Z, and/or an epitope, of the present invention) as determined by immunoassays well known in the art for assaying specific antibody-antigen binding. Antibodies of the invention include, but are not limited to, polyclonal, monoclonal, multispecific, human, humanized or chimeric antibodies, single chain antibodies, Fab fragments, F(ab′) fragments, fragments produced by a Fab expression library, anti-idiotypic (anti-Id) antibodies (including, e.g., anti-Id antibodies to antibodies of the invention), intracellularly-made antibodies (i.e., intrabodies), and epitope-binding fragments of any of the above. The term “antibody,” as used herein, refers to immunoglobulin molecules and immunologically active portions of immunoglobulin molecules, i.e., molecules that contain an antigen binding site that immunospecifically binds an antigen. The immunoglobulin molecules of the invention can be of any type (e.g., IgG, IgE, IgM, IgD, IgA and IgY), class (e.g., IgG1, IgG2, IgG3, IgG4, IgA1 and IgA2) or subclass of immunoglobulin molecule. In preferred embodiments, the immunoglobulin molecules of the invention are IgG1. In other preferred embodiments, the immunoglobulin molecules of the invention are IgG4.

Most preferably the antibodies are human antigen-binding antibody fragments of the present invention and include, but are not limited to, Fab, Fab′ and F(ab′)2, Fd, single-chain Fvs (scFv), single-chain antibodies, disulfide-linked Fvs (sdFv) and fragments comprising either a VL or VH domain. Antigen-binding antibody fragments, including single-chain antibodies, may comprise the variable region(s) alone or in combination with the entirety or a portion of the following: hinge region, CH1, CH2, and CH3 domains. Also included in the invention are antigen-binding fragments also comprising any combination of variable region(s) with a hinge region, CH1, CH2, and CH3 domains. The antibodies of the invention may be from any animal origin including birds and mammals. Preferably, the antibodies are human, murine (e.g., mouse and rat), donkey, ship rabbit, goat, guinea pig, camel, horse, or chicken. As used herein, “human” antibodies include antibodies having the amino acid sequence of a human immunoglobulin and include antibodies isolated from human immunoglobulin libraries or from animals transgenic for one or more human immunoglobulin and that do not express endogenous immunoglobulins, as described infra and, for example in, U.S. Pat. No. 5,939,598 by Kucherlapati et al.

The antibodies of the present invention may be monospecific, bispecific, trispecific or of greater multispecificity. Multispecific antibodies may be specific for different epitopes of a polypeptide of the present invention or may be specific for both a polypeptide of the present invention as well as for a heterologous epitope, such as a heterologous polypeptide or solid support material. See, e.g., PCT publications WO 93/17715; WO 92/08802; WO 91/00360; WO 92/05793; Tutt, et al., J. Immunol. 147:60-69 (1991); U.S. Pat. Nos. 4,474,893; 4,714,681; 4,925,648; 5,573,920; 5,601,819; Kostelny et al., J. Immunol. 148:1547-1553 (1992).

Antibodies of the present invention may be described or specified in terms of the epitope(s) or portion(s) of a polypeptide of the present invention which they recognize or specifically bind. The epitope(s) or polypeptide portion(s) may be specified as described herein, e.g., by N-terminal and C-terminal positions, or by size in contiguous amino acid residues, or listed in the Tables and Figures. Preferred epitopes of the invention include the predicted epitopes shown in column 7 of Table 1B.1, as well as polynucleotides that encode these epitopes. Antibodies which specifically bind any epitope or polypeptide of the present invention may also be excluded. Therefore, the present invention includes antibodies that specifically bind polypeptides of the present invention, and allows for the exclusion of the same.

Antibodies of the present invention may also be described or specified in terms of their cross-reactivity. Antibodies that do not bind any other analog, ortholog, or homolog of a polypeptide of the present invention are included. Antibodies that bind polypeptides with at least 95%, at least 90%, at least 85%, at least 80%, at least 75%, at least 70%, at least 65%, at least 60%, at least 55%, and at least 50% identity (as calculated using methods known in the art and described herein) to a polypeptide of the present invention are also included in the present invention. In specific embodiments, antibodies of the present invention cross-react with murine, rat and/or rabbit homologs of human proteins and the corresponding epitopes thereof. Antibodies that do not bind polypeptides with less than 95%, less than 90%, less than 85%, less than 80%, less than 75%, less than 70%, less than 65%, less than 60%, less than 55%, and less than 50% identity (as calculated using methods known in the art and described herein) to a polypeptide of the present invention are also included in the present invention. In a specific embodiment, the above-described cross-reactivity is with respect to any single specific antigenic or immunogenic polypeptide, or combination(s) of 2, 3, 4, 5, or more of the specific antigenic and/or immunogenic polypeptides disclosed herein. Further included in the present invention are antibodies which bind polypeptides encoded by polynucleotides which hybridize to a polynucleotide of the present invention under stringent hybridization conditions (as described herein). Antibodies of the present invention may also be described or specified in terms of their binding affinity to a polypeptide of the invention. Preferred binding affinities include those with a dissociation constant or Kd less than 5×10⁻² M, 10⁻² M, 5×10⁻³ M, 10⁻³ M, 5×10⁻⁴ M, 10⁻⁴ M, 5×10⁻⁵ M, 10⁻⁵ M, 5×10⁻⁶ M, 10⁻⁶M, 5×10⁻⁷ M, 10⁻⁷ M, 5×10⁻⁸ M, 10⁻⁸ M, 5×10⁻⁹ M, 10⁻⁹ M, 5×10⁻¹⁰ M, 10⁻¹⁰ M, 5×10⁻¹¹ M, 10⁻¹¹ M, 5×10⁻¹² M, 10⁻¹² M, 5×10¹³ M, 10⁻¹³ M, 5×10⁻¹⁴ M, 10⁻¹⁴ M, 5×10⁻¹⁵ M, or 10⁻¹⁵ M.

The invention also provides antibodies that competitively inhibit binding of an antibody to an epitope of the invention as determined by any method known in the art for determining competitive binding, for example, the immunoassays described herein. In preferred embodiments, the antibody competitively inhibits binding to the epitope by at least 95%, at least 90%, at least 85%, at least 80%, at least 75%, at least 70%, at least 60%, or at least 50%.

Antibodies of the present invention may act as agonists or antagonists of the polypeptides of the present invention. For example, the present invention includes antibodies which disrupt the receptor/ligand interactions with the polypeptides of the invention either partially or fully. Preferably, antibodies of the present invention bind an antigenic epitope disclosed herein, or a portion thereof. The invention features both receptor-specific antibodies and ligand-specific antibodies. The invention also features receptor-specific antibodies which do not prevent ligand binding but prevent receptor activation. Receptor activation (i.e., signaling) may be determined by techniques described herein or otherwise known in the art. For example, receptor activation can be determined by detecting the phosphorylation (e.g., tyrosine or serine/threonine) of the receptor or its substrate by immunoprecipitation followed by western blot analysis (for example, as described supra). In specific embodiments, antibodies are provided that inhibit ligand activity or receptor activity by at least 95%, at least 90%, at least 85%, at least 80%, at least 75%, at least 70%, at least 60%, or at least 50% of the activity in absence of the antibody.

The invention also features receptor-specific antibodies which both prevent ligand binding and receptor activation as well as antibodies that recognize the receptor-ligand complex, and, preferably, do not specifically recognize the unbound receptor or the unbound ligand. Likewise, included in the invention are neutralizing antibodies which bind the ligand and prevent binding of the ligand to the receptor, as well as antibodies which bind the ligand, thereby preventing receptor activation, but do not prevent the ligand from binding the receptor. Further included in the invention are antibodies which activate the receptor. These antibodies may act as receptor agonists, i.e., potentiate or activate either all or a subset of the biological activities of the ligand-mediated receptor activation, for example, by inducing dimerization of the receptor. The antibodies may be specified as agonists, antagonists or inverse agonists for biological activities comprising the specific biological activities of the peptides of the invention disclosed herein. The above antibody agonists can be made using methods known in the art. See, e.g., PCT publication WO 96/40281; U.S. Pat. No. 5,811,097; Deng et al., Blood 92(6):1981-1988 (1998); Chen et al., Cancer Res. 58(16):3668-3678 (1998); Harrop et al., J. Immunol. 161(4):1786-1794 (1998); Zhu et al., Cancer Res. 58(15):3209-3214 (1998); Yoon et al., J. Immunol. 160(7):3170-3179 (1998); Prat et al., J. Cell. Sci. 111(Pt2):237-247 (1998); Pitard et al., J. Immunol. Methods 205(2):177-190 (1997); Liautard et al., Cytokine 9(4):233-241 (1997); Carlson et al., J. Biol. Chem. 272(17):11295-11301 (1997); Taryman et al., Neuron 14(4):755-762 (1995); Muller et al., Structure 6(9):1153-1167 (1998); Bartunek et al., Cytokine 8(1):14-20 (1996) (which are all incorporated by reference herein in their entireties).

Antibodies of the present invention may be used, for example, to purify, detect, and target the polypeptides of the present invention, including both in vitro and in vivo diagnostic and therapeutic methods. For example, the antibodies have utility in immunoassays for qualitatively and quantitatively measuring levels of the polypeptides of the present invention in biological samples. See, e.g., Harlow et al., Antibodies: A Laboratory Manual, (Cold Spring Harbor Laboratory Press, 2nd ed. 1988); incorporated by reference herein in its entirety.

As discussed in more detail below, the antibodies of the present invention may be used either alone or in combination with other compositions. The antibodies may further be recombinantly fused to a heterologous polypeptide at the N- or C-terminus or chemically conjugated (including covalent and non-covalent conjugations) to polypeptides or other compositions. For example, antibodies of the present invention may be recombinantly fused or conjugated to molecules useful as labels in detection assays and effector molecules such as heterologous polypeptides, drugs, radionuclides, or toxins. See, e.g., PCT publications WO 92/08495; WO 91/14438; WO 89/12624; U.S. Pat. No. 5,314,995; and EP 396,387; the disclosures of which are incorporated herein by reference in their entireties.

The antibodies of the invention include derivatives that are modified, i.e., by the covalent attachment of any type of molecule to the antibody such that covalent attachment does not prevent the antibody from generating an anti-idiotypic response. For example, but not by way of limitation, the antibody derivatives include antibodies that have been modified, e.g., by glycosylation, acetylation, pegylation, phosphylation, amidation, derivatization by known protecting/blocking groups, proteolytic cleavage, linkage to a cellular ligand or other protein, etc. Any of numerous chemical modifications may be carried out by known techniques, including, but not limited to specific chemical cleavage, acetylation, formylation, metabolic synthesis of tunicamycin, etc. Additionally, the derivative may contain one or more non-classical amino acids.

The antibodies of the present invention may be generated by any suitable method known in the art. Polyclonal antibodies to an antigen-of-interest can be produced by various procedures well known in the art. For example, a polypeptide of the invention can be administered to various host animals including, but not limited to, rabbits, mice, rats, etc. to induce the production of sera containing polyclonal antibodies specific for the antigen. Various adjuvants may be used to increase the immunological response, depending on the host species, and include but are not limited to, Freund's (complete and incomplete), mineral gels such as aluminum hydroxide, surface active substances such as lysolecithin, pluronic polyols, polyanions, peptides, oil emulsions, keyhole limpet hemocyanins, dinitrophenol, and potentially useful human adjuvants such as BCG (bacille Calmette-Guerin) and corynebacterium parvum. Such adjuvants are also well known in the art.

Monoclonal antibodies can be prepared using a wide variety of techniques known in the art including the use of hybridoma, recombinant, and phage display technologies, or a combination thereof. For example, monoclonal antibodies can be produced using hybridoma techniques including those known in the art and taught, for example, in Harlow et al., Antibodies: A Laboratory Manual, (Cold Spring Harbor Laboratory Press, 2nd ed. 1988); Hammerling, et al., in: Monoclonal Antibodies and T-Cell Hybridomas 563-681 (Elsevier, N.Y., 1981) (said references incorporated by reference in their entireties). The term “monoclonal antibody” as used herein is not limited to antibodies produced through hybridoma technology. The term “monoclonal antibody” refers to an antibody that is derived from a single clone, including any eukaryotic, prokaryotic, or phage clone, and not the method by which it is produced.

Methods for producing and screening for specific antibodies using hybridoma technology are routine and well known in the art and are discussed in detail in the Examples. In a non-limiting example, mice can be immunized with a polypeptide of the invention or a cell expressing such peptide. Once an immune response is detected, e.g., antibodies specific for the antigen are detected in the mouse serum, the mouse spleen is harvested and splenocytes isolated. The splenocytes are then fused by well known techniques to any suitable myeloma cells, for example cells from cell line SP20 available from the ATCC™. Hybridomas are selected and cloned by limited dilution. The hybridoma clones are then assayed by methods known in the art for cells that secrete antibodies capable of binding a polypeptide of the invention. Ascites fluid, which generally contains high levels of antibodies, can be generated by immunizing mice with positive hybridoma clones.

Accordingly, the present invention provides methods of generating monoclonal antibodies as well as antibodies produced by the method comprising culturing a hybridoma cell secreting an antibody of the invention wherein, preferably, the hybridoma is generated by fusing splenocytes isolated from a mouse immunized with an antigen of the invention with myeloma cells and then screening the hybridomas resulting from the fusion for hybridoma clones that secrete an antibody able to bind a polypeptide of the invention.

Another well known method for producing both polyclonal and monoclonal human B cell lines is transformation using Epstein Barr Virus (EBV). Protocols for generating EBV-transformed B cell lines are commonly known in the art, such as, for example, the protocol outlined in Chapter 7.22 of Current Protocols in Immunology, Coligan et al., Eds., 1994, John Wiley & Sons, NY, which is hereby incorporated in its entirety by reference. The source of B cells for transformation is commonly human peripheral blood, but B cells for transformation may also be derived from other sources including, but not limited to, lymph nodes, tonsil, spleen, tumor tissue, and infected tissues. Tissues are generally made into single cell suspensions prior to EBV transformation. Additionally, steps may be taken to either physically remove or inactivate T cells (e.g., by treatment with cyclosporin A) in B cell-containing samples, because T cells from individuals seropositive for anti-EBV antibodies can suppress B cell immortalization by EBV.

In general, the sample containing human B cells is innoculated with EBV, and cultured for 3-4 weeks. A typical source of EBV is the culture supernatant of the B95-8 cell line (ATCC™ #VR-1492). Physical signs of EBV transformation can generally be seen towards the end of the 3-4 week culture period. By phase-contrast microscopy, transformed cells may appear large, clear, hairy and tend to aggregate in tight clusters of cells. Initially, EBV lines are generally polyclonal. However, over prolonged periods of cell cultures, EBV lines may become monoclonal or polyclonal as a result of the selective outgrowth of particular B cell clones. Alternatively, polyclonal EBV transformed lines may be subcloned (e.g., by limiting dilution culture) or fused with a suitable fusion partner and plated at limiting dilution to obtain monoclonal B cell lines. Suitable fusion partners for EBV transformed cell lines include mouse myeloma cell lines (e.g., SP2/0, X63-Ag8.653), heteromyeloma cell lines (human x mouse; e.g, SPAM-8, SBC-H20, and CB-F7), and human cell lines (e.g., GM 1500, SKO-007, RPMI 8226, and KR-4). Thus, the present invention also provides a method of generating polyclonal or monoclonal human antibodies against polypeptides of the invention or fragments thereof, comprising EBV-transformation of human B cells.

Antibody fragments which recognize specific epitopes may be generated by known techniques. For example, Fab and F(ab′)2 fragments of the invention may be produced by proteolytic cleavage of immunoglobulin molecules, using enzymes such as papain (to produce Fab fragments) or pepsin (to produce F(ab′)2 fragments). F(ab′)2 fragments contain the variable region, the light chain constant region and the CH1 domain of the heavy chain.

For example, the antibodies of the present invention can also be generated using various phage display methods known in the art. In phage display methods, functional antibody domains are displayed on the surface of phage particles which carry the polynucleotide sequences encoding them. In a particular embodiment, such phage can be utilized to display antigen binding domains expressed from a repertoire or combinatorial antibody library (e.g., human or murine). Phage expressing an antigen binding domain that binds the antigen of interest can be selected or identified with antigen, e.g., using labeled antigen or antigen bound or captured to a solid surface or bead. Phage used in these methods are typically filamentous phage including fd and M13 binding domains expressed from phage with Fab, Fv or disulfide stabilized Fv antibody domains recombinantly fused to either the phage gene III or gene VIII protein. Examples of phage display methods that can be used to make the antibodies of the present invention include those disclosed in Brinkman et al., J. Immunol. Methods 182:41-50 (1995); Ames et al., J. Immunol. Methods 184:177-186 (1995); Kettleborough et al., Eur. J. Immunol. 24:952-958 (1994); Persic et al., Gene 187 9-18 (1997); Burton et al., Advances in Immunology 57:191-280 (1994); PCT application No. PCT/GB91/01134; PCT publications WO 90/02809; WO 91/10737; WO 92/01047; WO 92/18619; WO 93/11236; WO 95/15982; WO 95/20401; and U.S. Pat. Nos. 5,698,426; 5,223,409; 5,403,484; 5,580,717; 5,427,908; 5,750,753; 5,821,047; 5,571,698; 5,427,908; 5,516,637; 5,780,225; 5,658,727; 5,733,743 and 5,969,108; each of which is incorporated herein by reference in its entirety.

As described in the above references, after phage selection, the antibody coding regions from the phage can be isolated and used to generate whole antibodies, including human antibodies, or any other desired antigen binding fragment, and expressed in any desired host, including mammalian cells, insect cells, plant cells, yeast, and bacteria, e.g., as described in detail below. For example, techniques to recombinantly produce Fab, Fab′ and F(ab′)2 fragments can also be employed using methods known in the art such as those disclosed in PCT publication WO 92/22324; Mullinax et al., BioTechniques 12(6):864-869 (1992); and Sawai et al., AJRI 34:26-34 (1995); and Better et al., Science 240:1041-1043 (1988) (said references incorporated by reference in their entireties).

Examples of techniques which can be used to produce single-chain Fvs and antibodies include those described in U.S. Pat. Nos. 4,946,778 and 5,258,498; Huston et al., Methods in Enzymology 203:46-88 (1991); Shu et al., PNAS 90:7995-7999 (1993); and Skerra et al., Science 240:1038-1040 (1988). For some uses, including in vivo use of antibodies in humans and in vitro detection assays, it may be preferable to use chimeric, humanized, or human antibodies. A chimeric antibody is a molecule in which different portions of the antibody are derived from different animal species, such as antibodies having a variable region derived from a murine monoclonal antibody and a human immunoglobulin constant region. Methods for producing chimeric antibodies are known in the art. See e.g., Morrison, Science 229:1202 (1985); Oi et al., BioTechniques 4:214 (1986); Gillies et al., (1989) J. Immunol. Methods 125:191-202; U.S. Pat. Nos. 5,807,715; 4,816,567; and 4,816,397, which are incorporated herein by reference in their entirety. Humanized antibodies are antibody molecules from non-human species antibody that binds the desired antigen having one or more complementarity determining regions (CDRs) from the non-human species and a framework regions from a human immunoglobulin molecule. Often, framework residues in the human framework regions will be substituted with the corresponding residue from the CDR donor antibody to alter, preferably improve, antigen binding. These framework substitutions are identified by methods well known in the art, e.g., by modeling of the interactions of the CDR and framework residues to identify framework residues important for antigen binding and sequence comparison to identify unusual framework residues at particular positions. (See, e.g., Queen et al., U.S. Pat. No. 5,585,089; Riechmann et al., Nature 332:323 (1988), which are incorporated herein by reference in their entireties.) Antibodies can be humanized using a variety of techniques known in the art including, for example, CDR-grafting (EP 239,400; PCT publication WO 91/09967; U.S. Pat. Nos. 5,225,539; 5,530,101; and 5,585,089), veneering or resurfacing (EP 592,106; EP 519,596; Padlan, Molecular Immunology 28(4/5):489-498 (1991); Studnicka et al., Protein Engineering 7(6):805-814 (1994); Roguska. et al., PNAS 91:969-973 (1994)), and chain shuffling (U.S. Pat. No. 5,565,332).

Completely human antibodies are particularly desirable for therapeutic treatment of human patients. Human antibodies can be made by a variety of methods known in the art including phage display methods described above using antibody libraries derived from human immunoglobulin sequences. See also, U.S. Pat. Nos. 4,444,887 and 4,716,111; and PCT publications WO 98/46645, WO 98/50433, WO 98/24893, WO 98/16654, WO 96/34096, WO 96/33735, and WO 91/10741; each of which is incorporated herein by reference in its entirety.

Human antibodies can also be produced using transgenic mice which are incapable of expressing functional endogenous immunoglobulins, but which can express human immunoglobulin genes. For example, the human heavy and light chain immunoglobulin gene complexes may be introduced randomly or by homologous recombination into mouse embryonic stem cells. Alternatively, the human variable region, constant region, and diversity region may be introduced into mouse embryonic stem cells in addition to the human heavy and light chain genes. The mouse heavy and light chain immunoglobulin genes may be rendered non-functional separately or simultaneously with the introduction of human immunoglobulin loci by homologous recombination. In particular, homozygous deletion of the JH region prevents endogenous antibody production. The modified embryonic stem cells are expanded and microinjected into blastocysts to produce chimeric mice. The chimeric mice are then bred to produce homozygous offspring which express human antibodies. The transgenic mice are immunized in the normal fashion with a selected antigen, e.g., all or a portion of a polypeptide of the invention. Monoclonal antibodies directed against the antigen can be obtained from the immunized, transgenic mice using conventional hybridoma technology. The human immunoglobulin transgenes harbored by the transgenic mice rearrange during B cell differentiation, and subsequently undergo class switching and somatic mutation. Thus, using such a technique, it is possible to produce therapeutically useful IgG, IgA, IgM and IgE antibodies. For an overview of this technology for producing human antibodies, see Lonberg and Huszar, Int. Rev. Immunol. 13:65-93 (1995). For a detailed discussion of this technology for producing human antibodies and human monoclonal antibodies and protocols for producing such antibodies, see, e.g., PCT publications WO 98/24893; WO 92/01047; WO 96/34096; WO 96/33735; European Patent No. 0 598 877; U.S. Pat. Nos. 5,413,923; 5,625,126; 5,633,425; 5,569,825; 5,661,016; 5,545,806; 5,814,318; 5,885,793; 5,916,771; 5,939,598; 6,075,181; and 6,114,598, which are incorporated by reference herein in their entirety. In addition, companies such as ABGENIX™, Inc. (Freemont, Calif.) and Genpharm (San Jose, Calif.) can be engaged to provide human antibodies directed against a selected antigen using technology similar to that described above.

Completely human antibodies which recognize a selected epitope can be generated using a technique referred to as “guided selection.” In this approach a selected non-human monoclonal antibody, e.g., a mouse antibody, is used to guide the selection of a completely human antibody recognizing the same epitope. (Jespers et al., Bio/technology 12:899-903 (1988)).

Further, antibodies to the polypeptides of the invention can, in turn, be utilized to generate anti-idiotype antibodies that “mimic” polypeptides of the invention using techniques well known to those skilled in the art. (See, e.g., Greenspan & Bona, FASEB J. 7(5):437-444; (1989) and Nissinoff, J. Immunol. 147(8):2429-2438 (1991)). For example, antibodies which bind to and competitively inhibit polypeptide multimerization and/or binding of a polypeptide of the invention to a ligand can be used to generate anti-idiotypes that “mimic” the polypeptide multimerization and/or binding domain and, as a consequence, bind to and neutralize polypeptide and/or its ligand. Such neutralizing anti-idiotypes or Fab fragments of such anti-idiotypes can be used in therapeutic regimens to neutralize polypeptide ligand(s)/receptor(s). For example, such anti-idiotypic antibodies can be used to bind a polypeptide of the invention and/or to bind its ligand(s)/receptor(s), and thereby block its biological activity. Alternatively, antibodies which bind to and enhance polypeptide multimerization and/or binding, and/or receptor/ligand multimerization, binding and/or signaling can be used to generate anti-idiotypes that function as agonists of a polypeptide of the invention and/or its ligand/receptor. Such agonistic anti-idiotypes or Fab fragments of such anti-idiotypes can be used in therapeutic regimens as agonists of the polypeptides of the invention or its ligand(s)/receptor(s). For example, such anti-idiotypic antibodies can be used to bind a polypeptide of the invention and/or to bind its ligand(s)/receptor(s), and thereby promote or enhance its biological activity.

Intrabodies of the invention can be produced using methods known in the art, such as those disclosed and reviewed in Chen et al., Hum. Gene Ther. 5:595-601 (1994); Marasco, W. A., Gene Ther. 4:11-15 (1997); Rondon and Marasco, Annu. Rev. Microbiol. 51:257-283 (1997); Proba et al., J. Mol. Biol. 275:245-253 (1998); Cohen et al., Oncogene 17:2445-2456 (1998); Ohage and Steipe, J. Mol. Biol. 291:1119-1128 (1999); Ohage et al., J. Mol. Biol. 291:1129-1134 (1999); Wirtz and Steipe, Protein Sci. 8:2245-2250 (1999); Zhu et al., J. Immunol. Methods 231:207-222 (1999); and references cited therein.

Polynucleotides Encoding Antibodies

The invention further provides polynucleotides comprising a nucleotide sequence encoding an antibody of the invention and fragments thereof. The invention also encompasses polynucleotides that hybridize under stringent or alternatively, under lower stringency hybridization conditions, e.g., as defined supra, to polynucleotides that encode an antibody, preferably, that specifically binds to a polypeptide of the invention, preferably, an antibody that binds to a polypeptide having the amino acid sequence of SEQ ID NO:Y, to a polypeptide encoded by a portion of SEQ ID NO:X as defined in columns 8 and 9 of Table 2, and/or to a polypeptide encoded by the cDNA contained in ATCC™ Deposit No:Z.

The polynucleotides may be obtained, and the nucleotide sequence of the polynucleotides determined, by any method known in the art. For example, if the nucleotide sequence of the antibody is known, a polynucleotide encoding the antibody may be assembled from chemically synthesized oligonucleotides (e.g., as described in Kutmeier et al., BioTechniques 17:242 (1994)), which, briefly, involves the synthesis of overlapping oligonucleotides containing portions of the sequence encoding the antibody, annealing and ligating of those oligonucleotides, and then amplification of the ligated oligonucleotides by PCR.

Alternatively, a polynucleotide encoding an antibody may be generated from nucleic acid from a suitable source. If a clone containing a nucleic acid encoding a particular antibody is not available, but the sequence of the antibody molecule is known, a nucleic acid encoding the immunoglobulin may be chemically synthesized or obtained from a suitable source (e.g., an antibody cDNA library, or a cDNA library generated from, or nucleic acid, preferably poly A+ RNA, isolated from, any tissue or cells expressing the antibody, such as hybridoma cells selected to express an antibody of the invention) by PCR amplification using synthetic primers hybridizable to the 3′ and 5′ ends of the sequence or by cloning using an oligonucleotide probe specific for the particular gene sequence to identify, e.g., a cDNA clone from a cDNA library that encodes the antibody. Amplified nucleic acids generated by PCR may then be cloned into replicable cloning vectors using any method well known in the art.

Once the nucleotide sequence and corresponding amino acid sequence of the antibody is determined, the nucleotide sequence of the antibody may be manipulated using methods well known in the art for the manipulation of nucleotide sequences, e.g., recombinant DNA techniques, site directed mutagenesis, PCR, etc. (see, for example, the techniques described in Sambrook et al., 1990, Molecular Cloning, A Laboratory Manual, 2d Ed., Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y. and Ausubel et al., eds., 1998, Current Protocols in Molecular Biology, John Wiley & Sons, NY, which are both incorporated by reference herein in their entireties), to generate antibodies having a different amino acid sequence, for example to create amino acid substitutions, deletions, and/or insertions.

In a specific embodiment, the amino acid sequence of the heavy and/or light chain variable domains may be inspected to identify the sequences of the complementarity determining regions (CDRs) by methods that are well know in the art, e.g., by comparison to known amino acid sequences of other heavy and light chain variable regions to determine the regions of sequence hypervariability. Using routine recombinant DNA techniques, one or more of the CDRs may be inserted within framework regions, e.g., into human framework regions to humanize a non-human antibody, as described supra. The framework regions may be naturally occurring or consensus framework regions, and preferably human framework regions (see, e.g., Chothia et al., J. Mol. Biol. 278: 457-479 (1998) for a listing of human framework regions). Preferably, the polynucleotide generated by the combination of the framework regions and CDRs encodes an antibody that specifically binds a polypeptide of the invention. Preferably, as discussed supra, one or more amino acid substitutions may be made within the framework regions, and, preferably, the amino acid substitutions improve binding of the antibody to its antigen. Additionally, such methods may be used to make amino acid substitutions or deletions of one or more variable region cysteine residues participating in an intrachain disulfide bond to generate antibody molecules lacking one or more intrachain disulfide bonds. Other alterations to the polynucleotide are encompassed by the present invention and within the skill of the art.

In addition, techniques developed for the production of “chimeric antibodies” (Morrison et al., Proc. Natl. Acad. Sci. 81:851-855 (1984); Neuberger et al., Nature 312:604-608 (1984); Takeda et al., Nature 314:452-454 (1985)) by splicing genes from a mouse antibody molecule of appropriate antigen specificity together with genes from a human antibody molecule of appropriate biological activity can be used. As described supra, a chimeric antibody is a molecule in which different portions are derived from different animal species, such as those having a variable region derived from a murine mAb and a human immunoglobulin constant region, e.g., humanized antibodies.

Alternatively, techniques described for the production of single chain antibodies (U.S. Pat. No. 4,946,778; Bird, Science 242:423-42 (1988); Huston et al., Proc. Natl. Acad. Sci. USA 85:5879-5883 (1988); and Ward et al., Nature 334:544-54 (1989)) can be adapted to produce single chain antibodies. Single chain antibodies are formed by linking the heavy and light chain fragments of the Fv region via an amino acid bridge, resulting in a single chain polypeptide. Techniques for the assembly of functional Fv fragments in E. coli may also be used (Skerra et al., Science 242:1038-1041 (1988)).

Methods of Producing Antibodies

The antibodies of the invention can be produced by any method known in the art for the synthesis of antibodies, in particular, by chemical synthesis or preferably, by recombinant expression techniques. Methods of producing antibodies include, but are not limited to, hybridoma technology, EBV transformation, and other methods discussed herein as well as through the use recombinant DNA technology, as discussed below.

Recombinant expression of an antibody of the invention, or fragment, derivative or analog thereof, (e.g., a heavy or light chain of an antibody of the invention or a single chain antibody of the invention), requires construction of an expression vector containing a polynucleotide that encodes the antibody. Once a polynucleotide encoding an antibody molecule or a heavy or light chain of an antibody, or portion thereof (preferably containing the heavy or light chain variable domain), of the invention has been obtained, the vector for the production of the antibody molecule may be produced by recombinant DNA technology using techniques well known in the art. Thus, methods for preparing a protein by expressing a polynucleotide containing an antibody encoding nucleotide sequence are described herein. Methods which are well known to those skilled in the art can be used to construct expression vectors containing antibody coding sequences and appropriate transcriptional and translational control signals. These methods include, for example, in vitro recombinant DNA techniques, synthetic techniques, and in vivo genetic recombination. The invention, thus, provides replicable vectors comprising a nucleotide sequence encoding an antibody molecule of the invention, or a heavy or light chain thereof, or a heavy or light chain variable domain, operably linked to a promoter. Such vectors may include the nucleotide sequence encoding the constant region of the antibody molecule (see, e.g., PCT Publication WO 86/05807; PCT Publication WO 89/01036; and U.S. Pat. No. 5,122,464) and the variable domain of the antibody may be cloned into such a vector for expression of the entire heavy or light chain.

The expression vector is transferred to a host cell by conventional techniques and the transfected cells are then cultured by conventional techniques to produce an antibody of the invention. Thus, the invention includes host cells containing a polynucleotide encoding an antibody of the invention, or a heavy or light chain thereof, or a single chain antibody of the invention, operably linked to a heterologous promoter. In preferred embodiments for the expression of double-chained antibodies, vectors encoding both the heavy and light chains may be co-expressed in the host cell for expression of the entire immunoglobulin molecule, as detailed below.

A variety of host-expression vector systems may be utilized to express the antibody molecules of the invention. Such host-expression systems represent vehicles by which the coding sequences of interest may be produced and subsequently purified, but also represent cells which may, when transformed or transfected with the appropriate nucleotide coding sequences, express an antibody molecule of the invention in situ. These include but are not limited to microorganisms such as bacteria (e.g., E. coli, B. subtilis) transformed with recombinant bacteriophage DNA, plasmid DNA or cosmid DNA expression vectors containing antibody coding sequences; yeast (e.g., Saccharomyces, Pichia) transformed with recombinant yeast expression vectors containing antibody coding sequences; insect cell systems infected with recombinant virus expression vectors (e.g., baculovirus) containing antibody coding sequences; plant cell systems infected with recombinant virus expression vectors (e.g., cauliflower mosaic virus, CaMV; tobacco mosaic virus, TMV) or transformed with recombinant plasmid expression vectors (e.g., Ti plasmid) containing antibody coding sequences; or mammalian cell systems (e.g., COS, CHO, BHK, 293, 3T3 cells) harboring recombinant expression constructs containing promoters derived from the genome of mammalian cells (e.g., metallothionein promoter) or from mammalian viruses (e.g., the adenovirus late promoter; the vaccinia virus 7.5K promoter). Preferably, bacterial cells such as Escherichia coli, and more preferably, eukaryotic cells, especially for the expression of whole recombinant antibody molecule, are used for the expression of a recombinant antibody molecule. For example, mammalian cells such as Chinese hamster ovary cells (CHO), in conjunction with a vector such as the major intermediate early gene promoter element from human cytomegalovirus is an effective expression system for antibodies (Foecking et al., Gene 45:101 (1986); Cockett et al., Bio/Technology 8:2 (1990)).

In bacterial systems, a number of expression vectors may be advantageously selected depending upon the use intended for the antibody molecule being expressed. For example, when a large quantity of such a protein is to be produced, for the generation of pharmaceutical compositions of an antibody molecule, vectors which direct the expression of high levels of fusion protein products that are readily purified may be desirable. Such vectors include, but are not limited, to the E. coli expression vector pUR278 (Ruther et al., EMBO J. 2:1791 (1983)), in which the antibody coding sequence may be ligated individually into the vector in frame with the lac Z coding region so that a fusion protein is produced; pIN vectors (Inouye & Inouye, Nucleic Acids Res. 13:3101-3109 (1985); Van Heeke & Schuster, J. Biol. Chem. 24:5503-5509 (1989)); and the like. pGEX vectors may also be used to express foreign polypeptides as fusion proteins with glutathione S-transferase (GST). In general, such fusion proteins are soluble and can easily be purified from lysed cells by adsorption and binding to matrix glutathione-agarose beads followed by elution in the presence of free glutathione. The pGEX vectors are designed to include thrombin or factor Xa protease cleavage sites so that the cloned target gene product can be released from the GST moiety.

In an insect system, Autographa californica nuclear polyhedrosis virus (AcNPV) is used as a vector to express foreign genes. The virus grows in Spodoptera frugiperda cells. The antibody coding sequence may be cloned individually into non-essential regions (for example the polyhedrin gene) of the virus and placed under control of an AcNPV promoter (for example the polyhedrin promoter).

In mammalian host cells, a number of viral-based expression systems may be utilized. In cases where an adenovirus is used as an expression vector, the antibody coding sequence of interest may be ligated to an adenovirus transcription/translation control complex, e.g., the late promoter and tripartite leader sequence. This chimeric gene may then be inserted in the adenovirus genome by in vitro or in vivo recombination. Insertion in a non-essential region of the viral genome (e.g., region E1 or E3) will result in a recombinant virus that is viable and capable of expressing the antibody molecule in infected hosts. (e.g., see Logan & Shenk, Proc. Natl. Acad. Sci. USA 81:355-359 (1984)). Specific initiation signals may also be required for efficient translation of inserted antibody coding sequences. These signals include the ATG initiation codon and adjacent sequences. Furthermore, the initiation codon must be in phase with the reading frame of the desired coding sequence to ensure translation of the entire insert. These exogenous translational control signals and initiation codons can be of a variety of origins, both natural and synthetic. The efficiency of expression may be enhanced by the inclusion of appropriate transcription enhancer elements, transcription terminators, etc. (see Bittner et al., Methods in Enzymol. 153:51-544 (1987)).

In addition, a host cell strain may be chosen which modulates the expression of the inserted sequences, or modifies and processes the gene product in the specific fashion desired. Such modifications (e.g., glycosylation) and processing (e.g., cleavage) of protein products may be important for the function of the protein. Different host cells have characteristic and specific mechanisms for the post-translational processing and modification of proteins and gene products. Appropriate cell lines or host systems can be chosen to ensure the correct modification and processing of the foreign protein expressed. To this end, eukaryotic host cells which possess the cellular machinery for proper processing of the primary transcript, glycosylation, and phosphorylation of the gene product may be used. Such mammalian host cells include but are not limited to CHO, VERY, BHK, Hela, COS, MDCK, 293, 3T3, W138, and in particular, breast cancer cell lines such as, for example, BT483, Hs578T, HTB2, BT20 and T47D, and normal mammary gland cell line such as, for example, CRL7030 and Hs578Bst.

For long-term, high-yield production of recombinant proteins, stable expression is preferred. For example, cell lines which stably express the antibody molecule may be engineered. Rather than using expression vectors which contain viral origins of replication, host cells can be transformed with DNA controlled by appropriate expression control elements (e.g., promoter, enhancer, sequences, transcription terminators, polyadenylation sites, etc.), and a selectable marker. Following the introduction of the foreign DNA, engineered cells may be allowed to grow for 1-2 days in an enriched media, and then are switched to a selective media. The selectable marker in the recombinant plasmid confers resistance to the selection and allows cells to stably integrate the plasmid into their chromosomes and grow to form foci which in turn can be cloned and expanded into cell lines. This method may advantageously be used to engineer cell lines which express the antibody molecule. Such engineered cell lines may be particularly useful in screening and evaluation of compounds that interact directly or indirectly with the antibody molecule.

A number of selection systems may be used, including but not limited to the herpes simplex virus thymidine kinase (Wigler et al., Cell 11:223 (1977)), hypoxanthine-guanine phosphoribosyltransferase (Szybalska & Szybalski, Proc. Natl. Acad. Sci. USA 48:202 (1992)), and adenine phosphoribosyltransferase (Lowy et al., Cell 22:817 (1980)) genes can be employed in tk−, hgprt− or aprt− cells, respectively. Also, antimetabolite resistance can be used as the basis of selection for the following genes: dhfr, which confers resistance to methotrexate (Wigler et al., Natl. Acad. Sci. USA 77:357 (1980); O'Hare et al., Proc. Natl. Acad. Sci. USA 78:1527 (1981)); gpt, which confers resistance to mycophenolic acid (Mulligan & Berg, Proc. Natl. Acad. Sci. USA 78:2072 (1981)); neo, which confers resistance to the aminoglycoside G-418 Clinical Pharmacy 12:488-505; Wu and Wu, Biotherapy 3:87-95 (1991); Tolstoshev, Ann. Rev. Pharmacol. Toxicol. 32:573-596 (1993); Mulligan, Science 260:926-932 (1993); and Morgan and Anderson, Ann. Rev. Biochem. 62:191-217 (1993); May, 1993, TIB TECH 11(5):155-215 (1993)); and hygro, which confers resistance to hygromycin (Santerre et al., Gene 30:147 (1984)). Methods commonly known in the art of recombinant DNA technology may be routinely applied to select the desired recombinant clone, and such methods are described, for example, in Ausubel et al. (eds.), Current Protocols in Molecular Biology, John Wiley & Sons, NY (1993); Kriegler, Gene Transfer and Expression, A Laboratory Manual, Stockton Press, NY (1990); and in Chapters 12 and 13, Dracopoli et al. (eds), Current Protocols in Human Genetics, John Wiley & Sons, NY (1994); Colberre-Garapin et al., J. Mol. Biol. 150:1 (1981), which are incorporated by reference herein in their entireties.

The expression levels of an antibody molecule can be increased by vector amplification (for a review, see Bebbington and Hentschel, The use of vectors based on gene amplification for the expression of cloned genes in mammalian cells in DNA cloning, Vol. 3. (Academic Press, New York, 1987)). When a marker in the vector system expressing antibody is amplifiable, increase in the level of inhibitor present in culture of host cell will increase the number of copies of the marker gene. Since the amplified region is associated with the antibody gene, production of the antibody will also increase (Crouse et al., Mol. Cell. Biol. 3:257 (1983)).

Vectors which use glutamine synthase (GS) or DHFR as the selectable markers can be amplified in the presence of the drugs methionine sulphoximine or methotrexate, respectively. An advantage of glutamine synthase based vectors are the availabilty of cell lines (e.g., the murine myeloma cell line, NSO) which are glutamine synthase negative. Glutamine synthase expression systems can also function in glutamine synthase expressing cells (e.g. Chinese Hamster Ovary (CHO) cells) by providing additional inhibitor to prevent the functioning of the endogenous gene. A glutamine synthase expression system and components thereof are detailed in PCT publications: WO87/04462; WO86/05807; WO89/01036; WO89/10404; and WO91/06657 which are incorporated in their entireties by reference herein. Additionally, glutamine synthase expression vectors that may be used according to the present invention are commercially available from suppliers, including, for example Lonza Biologics, Inc. (Portsmouth, N.H.). Expression and production of monoclonal antibodies using a GS expression system in murine myeloma cells is described in Bebbington et al., Bio/technology 10: 169 (1992) and in Biblia and Robinson Biotechnol. Prog. 11: 1 (1995) which are incorporated in their entireties by reference herein.

The host cell may be co-transfected with two expression vectors of the invention, the first vector encoding a heavy chain derived polypeptide and the second vector encoding a light chain derived polypeptide. The two vectors may contain identical selectable markers which enable equal expression of heavy and light chain polypeptides. Alternatively, a single vector may be used which encodes, and is capable of expressing, both heavy and light chain polypeptides. In such situations, the light chain should be placed before the heavy chain to avoid an excess of toxic free heavy chain (Proudfoot, Nature 322:52 (1986); Kohler, Proc. Natl. Acad. Sci. USA 77:2197 (1980)). The coding sequences for the heavy and light chains may comprise cDNA or genomic DNA.

Once an antibody molecule of the invention has been produced by an animal, chemically synthesized, or recombinantly expressed, it may be purified by any method known in the art for purification of an immunoglobulin molecule, for example, by chromatography (e.g., ion exchange, affinity, particularly by affinity for the specific antigen after Protein A, and sizing column chromatography), centrifugation, differential solubility, or by any other standard technique for the purification of proteins. In addition, the antibodies of the present invention or fragments thereof can be fused to heterologous polypeptide sequences described herein or otherwise known in the art, to facilitate purification.

The present invention encompasses antibodies recombinantly fused or chemically conjugated (including both covalently and non-covalently conjugations) to a polypeptide (or portion thereof, preferably at least 10, 20, 30, 40, 50, 60, 70, 80, 90 or 100 amino acids of the polypeptide) of the present invention to generate fusion proteins. The fusion does not necessarily need to be direct, but may occur through linker sequences. The antibodies may be specific for antigens other than polypeptides (or portion thereof, preferably at least 10, 20, 30, 40, 50, 60, 70, 80, 90 or 100 amino acids of the polypeptide) of the present invention. For example, antibodies may be used to target the polypeptides of the present invention to particular cell types, either in vitro or in vivo, by fusing or conjugating the polypeptides of the present invention to antibodies specific for particular cell surface receptors. Antibodies fused or conjugated to the polypeptides of the present invention may also be used in in vitro immunoassays and purification methods using methods known in the art. See e.g., Harbor et al., supra, and PCT publication WO 93/21232; EP 439,095; Naramura et al., Immunol. Lett. 39:91-99 (1994); U.S. Pat. No. 5,474,981; Gillies et al., PNAS 89:1428-1432 (1992); Fell et al., J. Immunol. 146:2446-2452 (1991), which are incorporated by reference in their entireties.

The present invention further includes compositions comprising the polypeptides of the present invention fused or conjugated to antibody domains other than the variable regions. For example, the polypeptides of the present invention may be fused or conjugated to an antibody Fc region, or portion thereof. The antibody portion fused to a polypeptide of the present invention may comprise the constant region, hinge region, CH1 domain, CH2 domain, and CH3 domain or any combination of whole domains or portions thereof. The polypeptides may also be fused or conjugated to the above antibody portions to form multimers. For example, Fc portions fused to the polypeptides of the present invention can form dimers through disulfide bonding between the Fc portions. Higher multimeric forms can be made by fusing the polypeptides to portions of IgA and IgM. Methods for fusing or conjugating the polypeptides of the present invention to antibody portions are known in the art. See, e.g., U.S. Pat. Nos. 5,336,603; 5,622,929; 5,359,046; 5,349,053; 5,447,851; 5,112,946; EP 307,434; EP 367,166; PCT publications WO 96/04388; WO 91/06570; Ashkenazi et al., Proc. Natl. Acad. Sci. USA 88:10535-10539 (1991); Zheng et al., J. Immunol. 154:5590-5600 (1995); and Vil et al., Proc. Natl. Acad. Sci. USA 89:11337-11341 (1992) (said references incorporated by reference in their entireties).

As discussed, supra, the polypeptides corresponding to a polypeptide, polypeptide fragment, or a variant of SEQ ID NO:Y may be fused or conjugated to the above antibody portions to increase the in vivo half life of the polypeptides or for use in immunoassays using methods known in the art. Further, the polypeptides corresponding to SEQ ID NO:Y may be fused or conjugated to the above antibody portions to facilitate purification. One reported example describes chimeric proteins consisting of the first two domains of the human CD4-polypeptide and various domains of the constant regions of the heavy or light chains of mammalian immunoglobulins. See EP 394,827; and Traunecker et al., Nature 331:84-86 (1988). The polypeptides of the present invention fused or conjugated to an antibody having disulfide-linked dimeric structures (due to the IgG) may also be more efficient in binding and neutralizing other molecules, than the monomeric secreted protein or protein fragment alone. See, for example, Fountoulakis et al., J. Biochem. 270:3958-3964 (1995). In many cases, the Fc part in a fusion protein is beneficial in therapy and diagnosis, and thus can result in, for example, improved pharmacokinetic properties. See, for example, EP A 232,262. Alternatively, deleting the Fc part after the fusion protein has been expressed, detected, and purified, would be desired. For example, the Fc portion may hinder therapy and diagnosis if the fusion protein is used as an antigen for immunizations. In drug discovery, for example, human proteins, such as hIL-5, have been fused with Fc portions for the purpose of high-throughput screening assays to identify antagonists of hIL-5. (See, Bennett et al., J. Molecular Recognition 8:52-58 (1995); Johanson et al., J. Biol. Chem. 270:9459-9471 (1995)).

Moreover, the antibodies or fragments thereof of the present invention can be fused to marker sequences, such as a peptide to facilitate purification. In preferred embodiments, the marker amino acid sequence is a hexa-histidine peptide, such as the tag provided in a pQE vector (QIAGEN, Inc., 9259 Eton Avenue, Chatsworth, Calif., 91311), among others, many of which are commercially available. As described in Gentz et al., Proc. Natl. Acad. Sci. USA 86:821-824 (1989), for instance, hexa-histidine provides for convenient purification of the fusion protein. Other peptide tags useful for purification include, but are not limited to, the “HA” tag, which corresponds to an epitope derived from the influenza hemagglutinin protein (Wilson et al., Cell 37:767 (1984)) and the “flag” tag.

The present invention further encompasses antibodies or fragments thereof conjugated to a diagnostic or therapeutic agent. The antibodies can be used diagnostically to, for example, monitor the development or progression of a tumor as part of a clinical testing procedure to, e.g., determine the efficacy of a given treatment regimen. Detection can be facilitated by coupling the antibody to a detectable substance. Examples of detectable substances include various enzymes, prosthetic groups, fluorescent materials, luminescent materials, bioluminescent materials, radioactive materials, positron emitting metals using various positron emission tomographies, and nonradioactive paramagnetic metal ions. The detectable substance may be coupled or conjugated either directly to the antibody (or fragment thereof) or indirectly, through an intermediate (such as, for example, a linker known in the art) using techniques known in the art. See, for example, U.S. Pat. No. 4,741,900 for metal ions which can be conjugated to antibodies for use as diagnostics according to the present invention. Examples of suitable enzymes include horseradish peroxidase, alkaline phosphatase, beta-galactosidase, or acetylcholinesterase; examples of suitable prosthetic group complexes include streptavidin/biotin and avidin/biotin; examples of suitable fluorescent materials include umbelliferone, fluorescein, fluorescein isothiocyanate, rhodamine, dichlorotriazinylamine fluorescein, dansyl chloride or phycoerythrin; an example of a luminescent material includes luminol; examples of bioluminescent materials include luciferase, luciferin, and aequorin; and examples of suitable radioactive material include 125I, 131I, 111In or 99Tc.

Further, an antibody or fragment thereof may be conjugated to a therapeutic moiety such as a cytotoxin, e.g., a cytostatic or cytocidal agent, a therapeutic agent or a radioactive metal ion, e.g., alpha-emitters such as, for example, 213Bi. A cytotoxin or cytotoxic agent includes any agent that is detrimental to cells. Examples include paclitaxol, cytochalasin B, gramicidin D, ethidium bromide, emetine, mitomycin, etoposide, tenoposide, vincristine, vinblastine, colchicin, doxorubicin, daunorubicin, dihydroxy anthracin dione, mitoxantrone, mithramycin, actinomycin D, 1-dehydrotestosterone, glucocorticoids, procaine, tetracaine, lidocaine, propranolol, and puromycin and analogs or homologs thereof. Therapeutic agents include, but are not limited to, antimetabolites (e.g., methotrexate, 6-mercaptopurine, 6-thioguanine, cytarabine, 5-fluorouracil decarbazine), alkylating agents (e.g., mechlorethamine, thioepa chlorambucil, melphalan, carmustine (BSNU) and lomustine (CCNU), cyclothosphamide, busulfan, dibromomannitol, streptozotocin, mitomycin C, and cis-dichlorodiamine platinum (II) (DDP) cisplatin), anthracyclines (e.g., daunorubicin (formerly daunomycin) and doxorubicin), antibiotics (e.g., dactinomycin (formerly actinomycin), bleomycin, mithramycin, and anthramycin (AMC)), and anti-mitotic agents (e.g., vincristine and vinblastine).

The conjugates of the invention can be used for modifying a given biological response, the therapeutic agent or drug moiety is not to be construed as limited to classical chemical therapeutic agents. For example, the drug moiety may be a protein or polypeptide possessing a desired biological activity. Such proteins may include, for example, a toxin such as abrin, ricin A, pseudomonas exotoxin, or diphtheria toxin; a protein such as tumor necrosis factor, a-interferon, β-interferon, nerve growth factor, platelet derived growth factor, tissue plasminogen activator, an apoptotic agent, e.g., TNF-alpha, TNF-beta, AIM I (See, International Publication No. WO 97/33899), AIM II (See, International Publication No. WO 97/34911), Fas Ligand (Takahashi et al., Int. Immunol, 6:1567-1574 (1994)), VEGI (See, International Publication No. WO 99/23105), a thrombotic agent or an anti-angiogenic agent, e.g., angiostatin or endostatin; or, biological response modifiers such as, for example, lymphokines, interleukin-1 (“IL-1”), interleukin-2 (“IL-2”), interleukin-6 (“IL-6”), granulocyte macrophage colony stimulating factor (“GM-CSF”), granulocyte colony stimulating factor (“G-CSF”), or other growth factors.

Antibodies may also be attached to solid supports, which are particularly useful for immunoassays or purification of the target antigen. Such solid supports include, but are not limited to, glass, cellulose, polyacrylamide, nylon, polystyrene, polyvinyl chloride or polypropylene.

Techniques for conjugating such therapeutic moiety to antibodies are well known. See, for example, Arnon et al., “Monoclonal Antibodies For Immunotargeting Of Drugs In Cancer Therapy”, in Monoclonal Antibodies And Cancer Therapy, Reisfeld et al. (eds.), pp. 243-56 (Alan R. Liss, Inc. 1985); Hellstrom et al., “Antibodies For Drug Delivery”, in Controlled Drug Delivery (2nd Ed.), Robinson et al. (eds.), pp. 623-53 (Marcel Dekker, Inc. 1987); Thorpe, “Antibody Carriers Of Cytotoxic Agents In Cancer Therapy: A Review”, in Monoclonal Antibodies '84: Biological And Clinical Applications, Pinchera et al. (eds.), pp. 475-506 (1985); “Analysis, Results, And Future Prospective Of The Therapeutic Use Of Radiolabeled Antibody In Cancer Therapy”, in Monoclonal Antibodies For Cancer Detection And Therapy, Baldwin et al. (eds.), pp. 303-16 (Academic Press 1985), and Thorpe et al., “The Preparation And Cytotoxic Properties Of Antibody-Toxin Conjugates”, Immunol. Rev. 62:119-58 (1982).

Alternatively, an antibody can be conjugated to a second antibody to form an antibody heteroconjugate as described by Segal in U.S. Pat. No. 4,676,980, which is incorporated herein by reference in its entirety.

An antibody, with or without a therapeutic moiety conjugated to it, administered alone or in combination with cytotoxic factor(s) and/or cytokine(s) can be used as a therapeutic.

Immunophenotyping

The antibodies of the invention may be utilized for immunophenotyping of cell lines and biological samples. Translation products of the gene of the present invention may be useful as cell-specific markers, or more specifically as cellular markers that are differentially expressed at various stages of differentiation and/or maturation of particular cell types. Monoclonal antibodies directed against a specific epitope, or combination of epitopes, will allow for the screening of cellular populations expressing the marker. Various techniques can be utilized using monoclonal antibodies to screen for cellular populations expressing the marker(s), and include magnetic separation using antibody-coated magnetic beads, “panning” with antibody attached to a solid matrix (i.e., plate), and flow cytometry (See, e.g., U.S. Pat. No. 5,985,660; and Morrison et al., Cell, 96:737-49 (1999)).

These techniques allow for the screening of particular populations of cells, such as might be found with hematological malignancies (i.e. minimal residual disease (MRD) in acute leukemic patients) and “non-self” cells in transplantations to prevent Graft-versus-Host Disease (GVHD). Alternatively, these techniques allow for the screening of hematopoietic stem and progenitor cells capable of undergoing proliferation and/or differentiation, as might be found in human umbilical cord blood.

Assays for Antibody Binding

The antibodies of the invention may be assayed for immunospecific binding by any method known in the art. The immunoassays which can be used include but are not limited to competitive and non-competitive assay systems using techniques such as western blots, radioimmunoassays, ELISA (enzyme linked immunosorbent assay), “sandwich” immunoassays, immunoprecipitation assays, precipitin reactions, gel diffusion precipitin reactions, immunodiffusion assays, agglutination assays, complement-fixation assays, immunoradiometric assays, fluorescent immunoassays, and protein A immunoassays, to name but a few. Such assays are routine and well known in the art (see, e.g., Ausubel et al., eds, 1994, Current Protocols in Molecular Biology, Vol. 1, John Wiley & Sons, Inc., New York, which is incorporated by reference herein in its entirety). Exemplary immunoassays are described briefly below (but are not intended by way of limitation).

Immunoprecipitation protocols generally comprise lysing a population of cells in a lysis buffer such as RIPA buffer (1% NP-40 or Triton X-100, 1% sodium deoxycholate, 0.1% SDS, 0.15 M NaCl, 0.01 M sodium phosphate at pH 7.2, 1% Trasylol) supplemented with protein phosphatase and/or protease inhibitors (e.g., EDTA, PMSF, aprotinin, sodium vanadate), adding the antibody of interest to the cell lysate, incubating for a period of time (e.g., 1-4 hours) at 4° C., adding protein A and/or protein G sepharose beads to the cell lysate, incubating for about an hour or more at 4° C., washing the beads in lysis buffer and resuspending the beads in SDS/sample buffer. The ability of the antibody of interest to immunoprecipitate a particular antigen can be assessed by, e.g., western blot analysis. One of skill in the art would be knowledgeable as to the parameters that can be modified to increase the binding of the antibody to an antigen and decrease the background (e.g., pre-clearing the cell lysate with sepharose beads). For further discussion regarding immunoprecipitation protocols see, e.g., Ausubel et al., eds., (1994), Current Protocols in Molecular Biology, Vol. 1, John Wiley & Sons, Inc., New York, section 10.16.1.

Western blot analysis generally comprises preparing protein samples, electrophoresis of the protein samples in a polyacrylamide gel (e.g., 8%-20% SDS-PAGE depending on the molecular weight of the antigen), transferring the protein sample from the polyacrylamide gel to a membrane such as nitrocellulose, PVDF or nylon, blocking the membrane in blocking solution (e.g., PBS with 3% BSA or non-fat milk), washing the membrane in washing buffer (e.g., PBS-Tween 20), blocking the membrane with primary antibody (the antibody of interest) diluted in blocking buffer, washing the membrane in washing buffer, blocking the membrane with a secondary antibody (which recognizes the primary antibody, e.g., an anti-human antibody) conjugated to an enzymatic substrate (e.g., horseradish peroxidase or alkaline phosphatase) or radioactive molecule (e.g., 32P or 125I) diluted in blocking buffer, washing the membrane in wash buffer, and detecting the presence of the antigen. One of skill in the art would be knowledgeable as to the parameters that can be modified to increase the signal detected and to reduce the background noise. For further discussion regarding western blot protocols see, e.g., Ausubel et al., eds, (1994), Current Protocols in Molecular Biology, Vol. 1, John Wiley & Sons, Inc., New York, section 10.8.1.

ELISAs comprise preparing antigen, coating the well of a 96 well microtiter plate with the antigen, adding the antibody of interest conjugated to a detectable compound such as an enzymatic substrate (e.g., horseradish peroxidase or alkaline phosphatase) to the well and incubating for a period of time, and detecting the presence of the antigen. In ELISAs the antibody of interest does not have to be conjugated to a detectable compound; instead, a second antibody (which recognizes the antibody of interest) conjugated to a detectable compound may be added to the well. Further, instead of coating the well with the antigen, the antibody may be coated to the well. In this case, a second antibody conjugated to a detectable compound may be added following the addition of the antigen of interest to the coated well. One of skill in the art would be knowledgeable as to the parameters that can be modified to increase the signal detected as well as other variations of ELISAs known in the art. For further discussion regarding ELISAs see, e.g., Ausubel et al., eds, (1994), Current Protocols in Molecular Biology, Vol. 1, John Wiley & Sons, Inc., New York, section 11.2.1.

The binding affinity of an antibody to an antigen and the off-rate of an antibody-antigen interaction can be determined by competitive binding assays. One example of a competitive binding assay is a radioimmunoassay comprising the incubation of labeled antigen (e.g., 3H or 125I) with the antibody of interest in the presence of increasing amounts of unlabeled antigen, and the detection of the antibody bound to the labeled antigen. The affinity of the antibody of interest for a particular antigen and the binding off-rates can be determined from the data by scatchard plot analysis. Competition with a second antibody can also be determined using radioimmunoassays. In this case, the antigen is incubated with antibody of interest conjugated to a labeled compound (e.g., 3H or 125I) in the presence of increasing amounts of an unlabeled second antibody.

Antibodies of the invention may be characterized using immunocytochemistry methods on cells (e.g., mammalian cells, such as CHO cells) transfected with a vector enabling the expression of an antigen or with vector alone using techniques commonly known in the art. Antibodies that bind antigen transfected cells, but not vector-only transfected cells, are antigen specific.

Therapeutic Uses

Table 1D also provides information regarding biological activities and preferred therapeutic uses (i.e. see, “Preferred Indications” column) for polynucleotides and polypeptides of the invention (including antibodies, agonists, and/or antagonists thereof). Table 1D also provides information regarding assays which may be used to test polynucleotides and polypeptides of the invention (including antibodies, agonists, and/or antagonists thereof) for the corresponding biological activities. The first column (“Gene No.”) provides the gene number in the application for each clone identifier. The second column (“cDNA ATCC™ Deposit No:Z”) provides the unique clone identifier for each clone as previously described and indicated in Table 1A, Table 1B, and Table 1C. The third column (“AA SEQ ID NO:Y”) indicates the Sequence Listing SEQ ID Number for polypeptide sequences encoded by the corresponding cDNA clones (also as indicated in Table 1A, Table 1B, and Table 2). The fourth column (“Biological Activity”) indicates a biological activity corresponding to the indicated polypeptides (or polynucleotides encoding said polypeptides). The fifth column (“Exemplary Activity Assay”) further describes the corresponding biological activity and also provides information pertaining to the various types of assays which may be performed to test, demonstrate, or quantify the corresponding biological activity.

The present invention is further directed to antibody-based therapies which involve administering antibodies of the invention to an animal, preferably a mammal, and most preferably a human, patient for treating one or more of the disclosed diseases, disorders, or conditions. Therapeutic compounds of the invention include, but are not limited to, antibodies of the invention (including fragments, analogs and derivatives thereof as described herein) and nucleic acids encoding antibodies of the invention (including fragments, analogs and derivatives thereof and anti-idiotypic antibodies as described herein). The antibodies of the invention can be used to detect, prevent, diagnose, prognosticate, treat, and/or ameliorate diseases, disorders or conditions associated with aberrant expression and/or activity of a polypeptide of the invention, including, but not limited to, cancer and other hyperproliferative diseases and disorders. The treatment and/or prevention of cancer and other hyperproliferative diseases and disorders associated with aberrant expression and/or activity of a polypeptide of the invention includes, but is not limited to, alleviating symptoms associated with cancer and other hyperproliferative diseases and disorders. Antibodies of the invention may be provided in pharmaceutically acceptable compositions as known in the art or as described herein.

In a specific and preferred embodiment, the present invention is directed to antibody-based therapies which involve administering antibodies of the invention to an animal, preferably a mammal, and most preferably a human, patient for treating cancer and other hyperproliferative diseases and disorders. Therapeutic compounds of the invention include, but are not limited to, antibodies of the invention (e.g., antibodies directed to the full length protein expressed on the cell surface of a mammalian cell; antibodies directed to an epitope of a polypeptide of the invention (such as, for example, a predicted linear epitope shown in column 7 of Table 1B.1; or a conformational epitope, including fragments, analogs and derivatives thereof as described herein) and nucleic acids encoding antibodies of the invention (including fragments, analogs and derivatives thereof and anti-idiotypic antibodies as described herein). The antibodies of the invention can be used to detect, diagnose, prevent, treat, prognosticate, and/or ameliorate cancer and other hyperproliferative diseases, disorders or conditions associated with aberrant expression and/or activity of a polypeptide of the invention. The treatment and/or prevention of cancer and other hyperproliferative diseases, disorders, or conditions associated with aberrant expression and/or activity of a polypeptide of the invention includes, but is not limited to, alleviating symptoms associated with those diseases, disorders or conditions. Antibodies of the invention may be provided in pharmaceutically acceptable compositions as known in the art or as described herein.

A summary of the ways in which the antibodies of the present invention may be used therapeutically includes binding polynucleotides or polypeptides of the present invention locally or systemically in the body or by direct cytotoxicity of the antibody, e.g. as mediated by complement (CDC) or by effector cells (ADCC). Some of these approaches are described in more detail below. Armed with the teachings provided herein, one of ordinary skill in the art will know how to use the antibodies of the present invention for diagnostic, monitoring or therapeutic purposes without undue experimentation.

The antibodies of this invention may be advantageously utilized in combination with other monoclonal or chimeric antibodies, or with lymphokines or hematopoietic growth factors (such as, e.g., IL-2, IL-3 and IL-7), for example, which serve to increase the number or activity of effector cells which interact with the antibodies.

The antibodies of the invention may be administered alone or in combination with other types of treatments (e.g., radiation therapy, chemotherapy, hormonal therapy, immunotherapy and anti-tumor agents). Generally, administration of products of a species origin or species reactivity (in the case of antibodies) that is the same species as that of the patient is preferred. Thus, in a preferred embodiment, human antibodies, fragments derivatives, analogs, or nucleic acids, are administered to a human patient for therapy or prophylaxis.

It is preferred to use high affinity and/or potent in vivo inhibiting and/or neutralizing antibodies against polypeptides or polynucleotides of the present invention, fragments or regions thereof, for both immunoassays directed to and therapy of cancer and other hyperproliferative diseases and disorders related to polynucleotides or polypeptides, including fragments thereof, of the present invention. Such antibodies, fragments, or regions, will preferably have an affinity for polynucleotides or polypeptides of the invention, including fragments thereof. Preferred binding affinities include those with a dissociation constant or Kd less than 5×10⁻² M, 10⁻² M, 5×10⁻³ M, 10⁻³ M, 5×10⁻⁴ M, 10⁻⁴ M, 5×10⁻⁵ M, 10⁻⁵ M, 5×10⁻⁶ M, 10⁻⁶ M, 5×10⁻⁷ M, 10⁻⁷ M, 5×10⁻⁸ M, 10⁻⁸ M, 5×10⁻⁹ M, 10⁻⁹ M, 5×10⁻¹⁰ M, 10⁻¹⁰ M, 5×10⁻¹¹ M, 10⁻¹¹ M, 5×10⁻¹² M, 10⁻¹² M, 5×10⁻¹³ M, 10⁻¹³ M, 5×10⁻¹⁴ M, 10⁻¹⁴ M, 5×10⁻¹⁵ M, and 10⁻¹⁵ M.

Gene Therapy

In a specific embodiment, nucleic acids comprising sequences encoding antibodies or functional derivatives thereof, are administered to treat, inhibit or prevent cancer and other hyperproliferative disease or disorder associated with aberrant expression and/or activity of a polypeptide of the invention, by way of gene therapy. Gene therapy refers to therapy performed by the administration to a subject of an expressed or expressible nucleic acid. In this embodiment of the invention, the nucleic acids produce their encoded protein that mediates a therapeutic effect.

Any of the methods for gene therapy available in the art can be used according to the present invention. Exemplary methods are described below.

For general reviews of the methods of gene therapy, see Goldspiel et al., Clinical Pharmacy 12:488-505 (1993); Wu and Wu, Biotherapy 3:87-95 (1991); Tolstoshev, Ann. Rev. Pharmacol. Toxicol. 32:573-596 (1993); Mulligan, Science 260:926-932 (1993); and Morgan and Anderson, Ann. Rev. Biochem. 62:191-217 (1993); May, TIBTECH 11(5):155-215 (1993). Methods commonly known in the art of recombinant DNA technology which can be used are described in Ausubel et al. (eds.), Current Protocols in Molecular Biology, John Wiley & Sons, NY (1993); and Kriegler, Gene Transfer and Expression, A Laboratory Manual, Stockton Press, NY (1990).

In a preferred embodiment, the compound comprises nucleic acid sequences encoding an antibody, said nucleic acid sequences being part of expression vectors that express the antibody or fragments or chimeric proteins or heavy or light chains thereof in a suitable host. In particular, such nucleic acid sequences have promoters operably linked to the antibody coding region, said promoter being inducible or constitutive, and, optionally, tissue-specific. In another particular embodiment, nucleic acid molecules are used in which the antibody coding sequences and any other desired sequences are flanked by regions that promote homologous recombination at a desired site in the genome, thus providing for intrachromosomal expression of the antibody encoding nucleic acids (Koller and Smithies, Proc. Natl. Acad. Sci. USA 86:8932-8935 (1989); Zijlstra et al., Nature 342:435-438 (1989). In specific embodiments, the expressed antibody molecule is a single chain antibody; alternatively, the nucleic acid sequences include sequences encoding both the heavy and light chains, or fragments thereof, of the antibody.

Delivery of the nucleic acids into a patient may be either direct, in which case the patient is directly exposed to the nucleic acid or nucleic acid-carrying vectors, or indirect, in which case, cells are first transformed with the nucleic acids in vitro, then transplanted into the patient. These two approaches are known, respectively, as in vivo or ex vivo gene therapy.

In a specific embodiment, the nucleic acid sequences are directly administered in vivo, where it is expressed to produce the encoded product. This can be accomplished by any of numerous methods known in the art, e.g., by constructing them as part of an appropriate nucleic acid expression vector and administering it so that they become intracellular, e.g., by infection using defective or attenuated retrovirals or other viral vectors (see U.S. Pat. No. 4,980,286), or by direct injection of naked DNA, or by use of microparticle bombardment (e.g., a gene gun; Biolistic, DUPONT™), or coating with lipids or cell-surface receptors or transfecting agents, encapsulation in liposomes, microparticles, or microcapsules, or by administering them in linkage to a peptide which is known to enter the nucleus, by administering it in linkage to a ligand subject to receptor-mediated endocytosis (see, e.g., Wu and Wu, J. Biol. Chem. 262:4429-4432 (1987)) (which can be used to target cell types specifically expressing the receptors), etc. In another embodiment, nucleic acid-ligand complexes can be formed in which the ligand comprises a fusogenic viral peptide to disrupt endosomes, allowing the nucleic acid to avoid lysosomal degradation. In yet another embodiment, the nucleic acid can be targeted in vivo for cell specific uptake and expression, by targeting a specific receptor (see, e.g., PCT Publications WO 92/06180; WO 92/22635; WO92/20316; WO93/14188, WO 93/20221). Alternatively, the nucleic acid can be introduced intracellularly and incorporated within host cell DNA for expression, by homologous recombination (Koller and Smithies, Proc. Natl. Acad. Sci. USA 86:8932-8935 (1989); Zijlstra et al., Nature 342:435-438 (1989)).

In a specific embodiment, viral vectors that contains nucleic acid sequences encoding an antibody of the invention are used. For example, a retroviral vector can be used (see Miller et al., Meth. Enzymol. 217:581-599 (1993)). These retroviral vectors contain the components necessary for the correct packaging of the viral genome and integration into the host cell DNA. The nucleic acid sequences encoding the antibody to be used in gene therapy are cloned into one or more vectors, which facilitates delivery of the gene into a patient. More detail about retroviral vectors can be found in Boesen et al., Biotherapy 6:291-302 (1994), which describes the use of a retroviral vector to deliver the mdr1 gene to hematopoietic stem cells in order to make the stem cells more resistant to chemotherapy. Other references illustrating the use of retroviral vectors in gene therapy are: Clowes et al., J. Clin. Invest. 93:644-651 (1994); Kiem et al., Blood 83:1467-1473 (1994); Salmons and Gunzberg, Human Gene Therapy 4:129-141 (1993); and Grossman and Wilson, Curr. Opin. in Genetics and Devel. 3:110-114 (1993).

Adenoviruses are other viral vectors that can be used in gene therapy. Adenoviruses are especially attractive vehicles for delivering genes to respiratory epithelia. Adenoviruses naturally infect respiratory epithelia where they cause a mild disease. Other targets for adenovirus-based delivery systems are liver, the central nervous system, endothelial cells, and muscle. Adenoviruses have the advantage of being capable of infecting non-dividing cells. Kozarsky and Wilson, Current Opinion in Genetics and Development 3:499-503 (1993) present a review of adenovirus-based gene therapy. Bout et al., Human Gene Therapy 5:3-10 (1994) demonstrated the use of adenovirus vectors to transfer genes to the respiratory epithelia of rhesus monkeys. Other instances of the use of adenoviruses in gene therapy can be found in Rosenfeld et al., Science 252:431-434 (1991); Rosenfeld et al., Cell 68:143-155 (1992); Mastrangeli et al., J. Clin. Invest. 91:225-234 (1993); PCT Publication WO94/12649; and Wang, et al., Gene Therapy 2:775-783 (1995). In a preferred embodiment, adenovirus vectors are used.

Adeno-associated virus (AAV) has also been proposed for use in gene therapy (Walsh et al., Proc. Soc. Exp. Biol. Med. 204:289-300 (1993); U.S. Pat. No. 5,436,146).

Another approach to gene therapy involves transferring a gene to cells in tissue culture by such methods as electroporation, lipofection, calcium phosphate mediated transfection, or viral infection. Usually, the method of transfer includes the transfer of a selectable marker to the cells. The cells are then placed under selection to isolate those cells that have taken up and are expressing the transferred gene. Those cells are then delivered to a patient.

In this embodiment, the nucleic acid is introduced into a cell prior to administration in vivo of the resulting recombinant cell. Such introduction can be carried out by any method known in the art, including but not limited to transfection, electroporation, microinjection, infection with a viral or bacteriophage vector containing the nucleic acid sequences, cell fusion, chromosome-mediated gene transfer, microcell-mediated gene transfer, spheroplast fusion, etc. Numerous techniques are known in the art for the introduction of foreign genes into cells (see, e.g., Loeffler and Behr, Meth. Enzymol. 217:599-618 (1993); Cohen et al., Meth. Enzymol. 217:618-644 (1993); Cline, Pharmac. Ther. 29:69-92m (1985) and may be used in accordance with the present invention, provided that the necessary developmental and physiological functions of the recipient cells are not disrupted. The technique should provide for the stable transfer of the nucleic acid to the cell, so that the nucleic acid is expressible by the cell and preferably heritable and expressible by its cell progeny.

The resulting recombinant cells can be delivered to a patient by various methods known in the art. Recombinant blood cells (e.g., hematopoietic stem or progenitor cells) are preferably administered intravenously. The amount of cells envisioned for use depends on the desired effect, patient state, etc., and can be determined by one skilled in the art.

Cells into which a nucleic acid can be introduced for purposes of gene therapy encompass any desired, available cell type, and include but are not limited to epithelial cells, endothelial cells, keratinocytes, fibroblasts, muscle cells, hepatocytes; blood cells such as T lymphocytes, B lymphocytes, monocytes, macrophages, neutrophils, eosinophils, megakaryocytes, granulocytes; various stem or progenitor cells, in particular hematopoietic stem or progenitor cells, e.g., as obtained from bone marrow, umbilical cord blood, peripheral blood, fetal liver, etc.

In a preferred embodiment, the cell used for gene therapy is autologous to the patient.

In an embodiment in which recombinant cells are used in gene therapy, nucleic acid sequences encoding an antibody are introduced into the cells such that they are expressible by the cells or their progeny, and the recombinant cells are then administered in vivo for therapeutic effect. In a specific embodiment, stem or progenitor cells are used. Any stem and/or progenitor cells which can be isolated and maintained in vitro can potentially be used in accordance with this embodiment of the present invention (see e.g. PCT Publication WO 94/08598; Stemple and Anderson, Cell 71:973-985 (1992); Rheinwald, Meth. Cell Bio. 21A:229 (1980); and Pittelkow and Scott, Mayo Clinic Proc. 61:771 (1986)).

In a specific embodiment, the nucleic acid to be introduced for purposes of gene therapy comprises an inducible promoter operably linked to the coding region, such that expression of the nucleic acid is controllable by the presence or absence of an appropriate inducer of transcription.

Demonstration of Therapeutic or Prophylactic Activity

The compounds or pharmaceutical compositions of the invention are preferably tested in vitro, and then in vivo for the desired therapeutic or prophylactic activity, prior to use in humans. For example, in vitro assays to demonstrate the therapeutic or prophylactic utility of a compound or pharmaceutical composition include, the effect of a compound on a cell line or a patient tissue sample. The effect of the compound or composition on the cell line and/or tissue sample can be determined utilizing techniques known to those of skill in the art including, but not limited to, rosette formation assays and cell lysis assays. In accordance with the invention, in vitro assays which can be used to determine whether administration of a specific compound is indicated, include in vitro cell culture assays in which a patient tissue sample is grown in culture, and exposed to or otherwise administered a compound, and the effect of such compound upon the tissue sample is observed.

Therapeutic/Prophylactic Administration and Composition

The invention provides methods of treatment, inhibition and prophylaxis by administration to a subject of an effective amount of a compound or pharmaceutical composition of the invention, preferably a polypeptide or antibody of the invention. In a preferred embodiment, the compound is substantially purified (e.g., substantially free from substances that limit its effect or produce undesired side-effects). The subject is preferably an animal, including but not limited to animals such as cows, pigs, horses, chickens, cats, dogs, etc., and is preferably a mammal, and most preferably human.

Formulations and methods of administration that can be employed when the compound comprises a nucleic acid or an immunoglobulin are described above; additional appropriate formulations and routes of administration can be selected from among those described herein below.

Various delivery systems are known and can be used to administer a compound of the invention, e.g., encapsulation in liposomes, microparticles, microcapsules, recombinant cells capable of expressing the compound, receptor-mediated endocytosis (see, e.g., Wu and Wu, J. Biol. Chem. 262:4429-4432 (1987)), construction of a nucleic acid as part of a retroviral or other vector, etc. Methods of introduction include but are not limited to intradermal, intramuscular, intraperitoneal, intravenous, subcutaneous, intranasal, epidural, and oral routes. The compounds or compositions may be administered by any convenient route, for example by infusion or bolus injection, by absorption through epithelial or mucocutaneous linings (e.g., oral mucosa, rectal and intestinal mucosa, etc.) and may be administered together with other biologically active agents. Administration can be systemic or local. In addition, it may be desirable to introduce the pharmaceutical compounds or compositions of the invention into the central nervous system by any suitable route, including intraventricular and intrathecal injection; intraventricular injection may be facilitated by an intraventricular catheter, for example, attached to a reservoir, such as an Ommaya reservoir. Pulmonary administration can also be employed, e.g., by use of an inhaler or nebulizer, and formulation with an aerosolizing agent.

In a specific embodiment, it may be desirable to administer the pharmaceutical compounds or compositions of the invention locally to the area in need of treatment; this may be achieved by, for example, and not by way of limitation, local infusion during surgery, topical application, e.g., in conjunction with a wound dressing after surgery, by injection, by means of a catheter, by means of a suppository, or by means of an implant, said implant being of a porous, non-porous, or gelatinous material, including membranes, such as sialastic membranes, or fibers. Preferably, when administering a protein, including an antibody, of the invention, care must be taken to use materials to which the protein does not absorb.

In another embodiment, the compound or composition can be delivered in a vesicle, in particular a liposome (see Langer, Science 249:1527-1533 (1990); Treat et al., in Liposomes in the Therapy of Infectious Disease and Cancer, Lopez-Berestein and Fidler (eds.), Liss, New York, pp. 353-365 (1989); Lopez-Berestein, ibid., pp. 317-327; see generally ibid.)

In yet another embodiment, the compound or composition can be delivered in a controlled release system. In one embodiment, a pump may be used (see Langer, supra; Sefton, CRC Crit. Ref. Biomed. Eng. 14:201 (1987); Buchwald et al., Surgery 88:507 (1980); Saudek et al., N. Engl. J. Med. 321:574 (1989)). In another embodiment, polymeric materials can be used (see Medical Applications of Controlled Release, Langer and Wise (eds.), CRC Pres., Boca Raton, Fla. (1974); Controlled Drug Bioavailability, Drug Product Design and Performance, Smolen and Ball (eds.), Wiley, New York (1984); Ranger and Peppas, J., Macromol. Sci. Rev. Macromol. Chem. 23:61 (1983); see also Levy et al., Science 228:190 (1985); During et al., Ann. Neurol. 25:351 (1989); Howard et al., J. Neurosurg. 71:105 (1989)). In yet another embodiment, a controlled release system can be placed in proximity of the therapeutic target, e.g., the brain, thus requiring only a fraction of the systemic dose (see, e.g., Goodson, in Medical Applications of Controlled Release, supra, vol. 2, pp. 115-138 (1984)).

Other controlled release systems are discussed in the review by Langer (Science 249:1527-1533 (1990)).

In a specific embodiment where the compound of the invention is a nucleic acid encoding a protein, the nucleic acid can be administered in vivo to promote expression of its encoded protein, by constructing it as part of an appropriate nucleic acid expression vector and administering it so that it becomes intracellular, e.g., by use of a retroviral vector (see U.S. Pat. No. 4,980,286), or by direct injection, or by use of microparticle bombardment (e.g., a gene gun; Biolistic, DUPONT™), or coating with lipids or cell-surface receptors or transfecting agents, or by administering it in linkage to a homeobox-like peptide which is known to enter the nucleus (see e.g., Joliot et al., Proc. Natl. Acad. Sci. USA 88:1864-1868 (1991)), etc. Alternatively, a nucleic acid can be introduced intracellularly and incorporated within host cell DNA for expression, by homologous recombination.

The present invention also provides pharmaceutical compositions. Such compositions comprise a therapeutically effective amount of a compound, and a pharmaceutically acceptable carrier. In a specific embodiment, the term “pharmaceutically acceptable” means approved by a regulatory agency of the Federal or a state government or listed in the U.S. Pharmacopeia or other generally recognized pharmacopeia for use in animals, and more particularly in humans. The term “carrier” refers to a diluent, adjuvant, excipient, or vehicle with which the therapeutic is administered. Such pharmaceutical carriers can be sterile liquids, such as water and oils, including those of petroleum, animal, vegetable or synthetic origin, such as peanut oil, soybean oil, mineral oil, sesame oil and the like. Water is a preferred carrier when the pharmaceutical composition is administered intravenously. Saline solutions and aqueous dextrose and glycerol solutions can also be employed as liquid carriers, particularly for injectable solutions. Suitable pharmaceutical excipients include starch, glucose, lactose, sucrose, gelatin, malt, rice, flour, chalk, silica gel, sodium stearate, glycerol monostearate, talc, sodium chloride, dried skim milk, glycerol, propylene, glycol, water, ethanol and the like. The composition, if desired, can also contain minor amounts of wetting or emulsifying agents, or pH buffering agents. These compositions can take the form of solutions, suspensions, emulsion, tablets, pills, capsules, powders, sustained-release formulations and the like. The composition can be formulated as a suppository, with traditional binders and carriers such as triglycerides. Oral formulation can include standard carriers such as pharmaceutical grades of mannitol, lactose, starch, magnesium stearate, sodium saccharine, cellulose, magnesium carbonate, etc. Examples of suitable pharmaceutical carriers are described in “Remington's Pharmaceutical Sciences” by E.W. Martin. Such compositions will contain a therapeutically effective amount of the compound, preferably in purified form, together with a suitable amount of carrier so as to provide the form for proper administration to the patient. The formulation should suit the mode of administration.

In a preferred embodiment, the composition is formulated in accordance with routine procedures as a pharmaceutical composition adapted for intravenous administration to human beings. Typically, compositions for intravenous administration are solutions in sterile isotonic aqueous buffer. Where necessary, the composition may also include a solubilizing agent and a local anesthetic such as lignocaine to ease pain at the site of the injection. Generally, the ingredients are supplied either separately or mixed together in unit dosage form, for example, as a dry lyophilized powder or water free concentrate in a hermetically sealed container such as an ampoule or sachette indicating the quantity of active agent. Where the composition is to be administered by infusion, it can be dispensed with an infusion bottle containing sterile pharmaceutical grade water or saline. Where the composition is administered by injection, an ampoule of sterile water for injection or saline can be provided so that the ingredients may be mixed prior to administration.

The compounds of the invention can be formulated as neutral or salt forms. Pharmaceutically acceptable salts include those formed with anions such as those derived from hydrochloric, phosphoric, acetic, oxalic, tartaric acids, etc., and those formed with cations such as those derived from sodium, potassium, ammonium, calcium, ferric hydroxides, isopropylamine, triethylamine, 2-ethylamino ethanol, histidine, procaine, etc.

The amount of the compound of the invention which will be effective in the treatment, inhibition and prevention of a disease or disorder associated with aberrant expression and/or activity of a polypeptide of the invention can be determined by standard clinical techniques. In addition, in vitro assays may optionally be employed to help identify optimal dosage ranges. The precise dose to be employed in the formulation will also depend on the route of administration, and the seriousness of the disease or disorder, and should be decided according to the judgment of the practitioner and each patient's circumstances. Effective doses may be extrapolated from dose-response curves derived from in vitro or animal model test systems.

For antibodies, the dosage administered to a patient is typically 0.1 mg/kg to 100 mg/kg of the patient's body weight. Preferably, the dosage administered to a patient is between 0.1 mg/kg and 20 mg/kg of the patient's body weight, more preferably 1 mg/kg to 10 mg/kg of the patient's body weight. Generally, human antibodies have a longer half-life within the human body than antibodies from other species due to the immune response to the foreign polypeptides. Thus, lower dosages of human antibodies and less frequent administration is often possible. Further, the dosage and frequency of administration of antibodies of the invention may be reduced by enhancing uptake and tissue penetration (e.g., into the brain) of the antibodies by modifications such as, for example, lipidation.

The invention also provides a pharmaceutical pack or kit comprising one or more containers filled with one or more of the ingredients of the pharmaceutical compositions of the invention. Optionally associated with such container(s) can be a notice in the form prescribed by a governmental agency regulating the manufacture, use or sale of pharmaceuticals or biological products, which notice reflects approval by the agency of manufacture, use or sale for human administration.

Diagnosis and Imaging

Labeled antibodies, and derivatives and analogs thereof, which specifically bind to a polypeptide of interest can be used for diagnostic purposes to detect, diagnose, prognosticate, or monitor cancer and other hyperproliferative diseases, disorders, and/or conditions associated with the aberrant expression and/or activity of a polypeptide of the invention. The invention provides for the detection of aberrant expression of a polypeptide of interest, comprising (a) assaying the expression of the polypeptide of interest in cells or body fluid of an individual using one or more antibodies specific to the polypeptide interest and (b) comparing the level of gene expression with a standard gene expression level, whereby an increase or decrease in the assayed polypeptide gene expression level compared to the standard expression level is indicative of aberrant expression.

The invention provides a diagnostic assay for diagnosing cancer and other hyperproliferative disease or disorder, comprising (a) assaying the expression of the polypeptide of interest in cells or body fluid of an individual using one or more antibodies specific to the polypeptide interest and (b) comparing the level of gene expression with a standard gene expression level, whereby an increase or decrease in the assayed polypeptide gene expression level compared to the standard expression level is indicative of a particular cancer or other hyperproliferative disease or disorder. With respect to cancer and other hyperproliferative diseases and disorders, the presence of a relatively high amount of transcript in biopsied tissue from an individual may indicate a predisposition for the development of the disease, or may provide a means for detecting the disease prior to the appearance of actual clinical symptoms. A more definitive diagnosis of this type may allow health professionals to employ preventative measures or aggressive treatment earlier thereby preventing the development or further progression of the cancer or other hyperproliferative disease.

Antibodies of the invention can be used to assay protein levels in a biological sample using classical immunohistological methods known to those of skill in the art (e.g., see Jalkanen et al., J. Cell. Biol. 101:976-985 (1985); Jalkanen et al., J. Cell. Biol. 105:3087-3096 (1987)). Other antibody-based methods useful for detecting protein gene expression include immunoassays, such as the enzyme linked immunosorbent assay (ELISA) and the radioimmunoassay (RIA). Suitable antibody assay labels are known in the art and include enzyme labels, such as, glucose oxidase; radioisotopes, such as iodine (125I, 121I), carbon (14C), sulfur (35S), tritium (3H), indium (112In), and technetium (99Tc); luminescent labels, such as luminol; and fluorescent labels, such as fluorescein and rhodamine, and biotin.

One facet of the invention is the detection and diagnosis of a disease or disorder associated with aberrant expression of a polypeptide of interest in an animal, preferably a mammal and most preferably a human. In one embodiment, diagnosis comprises: a) administering (for example, parenterally, subcutaneously, or intraperitoneally) to a subject an effective amount of a labeled molecule which specifically binds to the polypeptide of interest; b) waiting for a time interval following the administering for permitting the labeled molecule to preferentially concentrate at sites in the subject where the polypeptide is expressed (and for unbound labeled molecule to be cleared to background level); c) determining background level; and d) detecting the labeled molecule in the subject, such that detection of labeled molecule above the background level indicates that the subject has a particular disease or disorder associated with aberrant expression of the polypeptide of interest. Background level can be determined by various methods including, comparing the amount of labeled molecule detected to a standard value previously determined for a particular system.

It will be understood in the art that the size of the subject and the imaging system used will determine the quantity of imaging moiety needed to produce diagnostic images. In the case of a radioisotope moiety, for a human subject, the quantity of radioactivity injected will normally range from about 5 to 20 millicuries of 99mTc. The labeled antibody or antibody fragment will then preferentially accumulate at the location of cells which contain the specific protein. In vivo tumor imaging is described in S. W. Burchiel et al., “Immunopharmacokinetics of Radiolabeled Antibodies and Their Fragments.” (Chapter 13 in Tumor Imaging: The Radiochemical Detection of Cancer, S. W. Burchiel and B. A. Rhodes, eds., Masson Publishing Inc. (1982)).

Depending on several variables, including the type of label used and the mode of administration, the time interval following the administration for permitting the labeled molecule to preferentially concentrate at sites in the subject and for unbound labeled molecule to be cleared to background level is 6 to 48 hours or 6 to 24 hours or 6 to 12 hours. In another embodiment the time interval following administration is 5 to 20 days or 5 to 10 days.

In an embodiment, monitoring of the disease or disorder is carried out by repeating the method for diagnosing the disease or disease, for example, one month after initial diagnosis, six months after initial diagnosis, one year after initial diagnosis, etc.

Presence of the labeled molecule can be detected in the patient using methods known in the art for in vivo scanning. These methods depend upon the type of label used. Skilled artisans will be able to determine the appropriate method for detecting a particular label. Methods and devices that may be used in the diagnostic methods of the invention include, but are not limited to, computed tomography (CT), whole body scan such as position emission tomography (PET), magnetic resonance imaging (MRI), and sonography.

In a specific embodiment, the molecule is labeled with a radioisotope and is detected in the patient using a radiation responsive surgical instrument (Thurston et al., U.S. Pat. No. 5,441,050). In another embodiment, the molecule is labeled with a fluorescent compound and is detected in the patient using a fluorescence responsive scanning instrument. In another embodiment, the molecule is labeled with a positron emitting metal and is detected in the patent using positron emission-tomography. In yet another embodiment, the molecule is labeled with a paramagnetic label and is detected in a patient using magnetic resonance imaging (MRI).

Kits

The present invention provides kits that can be used in the above methods. In one embodiment, a kit comprises an antibody of the invention, preferably a purified antibody, in one or more containers. In a specific embodiment, the kits of the present invention contain a substantially isolated polypeptide comprising an epitope which is specifically immunoreactive with an antibody included in the kit. Preferably, the kits of the present invention further comprise a control antibody which does not react with the polypeptide of interest. In another specific embodiment, the kits of the present invention contain a means for detecting the binding of an antibody to a polypeptide of interest (e.g., the antibody may be conjugated to a detectable substrate such as a fluorescent compound, an enzymatic substrate, a radioactive compound or a luminescent compound, or a second antibody which recognizes the first antibody may be conjugated to a detectable substrate).

In another specific embodiment of the present invention, the kit is a diagnostic kit for use in screening serum containing antibodies specific against proliferative and/or cancerous polynucleotides and polypeptides. Such a kit may include a control antibody that does not react with the polypeptide of interest. Such a kit may include a substantially isolated polypeptide antigen comprising an epitope which is specifically immunoreactive with at least one anti-polypeptide antigen antibody. Further, such a kit includes means for detecting the binding of said antibody to the antigen (e.g., the antibody may be conjugated to a fluorescent compound such as fluorescein or rhodamine which can be detected by flow cytometry). In specific embodiments, the kit may include a recombinantly produced or chemically synthesized polypeptide antigen. The polypeptide antigen of the kit may also be attached to a solid support.

In a more specific embodiment the detecting means of the above-described kit includes a solid support to which said polypeptide antigen is attached. Such a kit may also include a non-attached reporter-labeled anti-human antibody. In this embodiment, binding of the antibody to the polypeptide antigen can be detected by binding of the said reporter-labeled antibody.

In an additional embodiment, the invention includes a diagnostic kit for use in screening serum containing antigens of the polypeptide of the invention. The diagnostic kit includes a substantially isolated antibody specifically immunoreactive with polypeptide or polynucleotide antigens, and means for detecting the binding of the polynucleotide or polypeptide antigen to the antibody. In one embodiment, the antibody is attached to a solid support. In a specific embodiment, the antibody may be a monoclonal antibody. The detecting means of the kit may include a second, labeled monoclonal antibody. Alternatively, or in addition, the detecting means may include a labeled, competing antigen.

In one diagnostic configuration, test serum is reacted with a solid phase reagent having a surface-bound antigen obtained by the methods of the present invention. After binding with specific antigen antibody to the reagent and removing unbound serum components by washing, the reagent is reacted with reporter-labeled anti-human antibody to bind reporter to the reagent in proportion to the amount of bound anti-antigen antibody on the solid support. The reagent is again washed to remove unbound labeled antibody, and the amount of reporter associated with the reagent is determined. Typically, the reporter is an enzyme which is detected by incubating the solid phase in the presence of a suitable fluorometric, luminescent or calorimetric substrate (SIGMA™, St. Louis, Mo.).

The solid surface reagent in the above assay is prepared by known techniques for attaching protein material to solid support material, such as polymeric beads, dip sticks, 96-well plate or filter material. These attachment methods generally include non-specific adsorption of the protein to the support or covalent attachment of the protein, typically through a free amine group, to a chemically reactive group on the solid support, such as an activated carboxyl, hydroxyl, or aldehyde group. Alternatively, streptavidin coated plates can be used in conjunction with biotinylated antigen(s).

Thus, the invention provides an assay system or kit for carrying out this diagnostic method. The kit generally includes a support with surface-bound recombinant antigens, and a reporter-labeled anti-human antibody for detecting surface-bound anti-antigen antibody.

Uses of the Polynucleotides

Each of the polynucleotides identified herein can be used in numerous ways as reagents. The following description should be considered exemplary and utilizes known techniques.

The polynucleotides of the present invention are useful for chromosome identification. There exists an ongoing need to identify new chromosome markers, since few chromosome marking reagents, based on actual sequence data (repeat polymorphisms), are presently available. Each sequence is specifically targeted to and can hybridize with a particular location on an individual human chromosome, thus each polynucleotide of the present invention can routinely be used as a chromosome marker using techniques known in the art. Table 1B.1, column 8 provides the chromosome location of some of the polynucleotides of the invention.

Briefly, sequences can be mapped to chromosomes by preparing PCR primers (preferably at least 15 bp (e.g., 15-25 bp) from the sequences shown in SEQ ID NO:X. Primers can optionally be selected using computer analysis so that primers do not span more than one predicted exon in the genomic DNA. These primers are then used for PCR screening of somatic cell hybrids containing individual human chromosomes. Only those hybrids containing the human gene corresponding to SEQ ID NO:X will yield an amplified fragment.

Similarly, somatic hybrids provide a rapid method of PCR mapping the polynucleotides to particular chromosomes. Three or more clones can be assigned per day using a single thermal cycler. Moreover, sublocalization of the polynucleotides can be achieved with panels of specific chromosome fragments. Other gene mapping strategies that can be used include in situ hybridization, prescreening with labeled flow-sorted chromosomes, preselection by hybridization to construct chromosome specific-cDNA libraries, and computer mapping techniques (See, e.g., Shuler, Trends Biotechnol 16:456-459 (1998) which is hereby incorporated by reference in its entirety).

Precise chromosomal location of the polynucleotides can also be achieved using fluorescence in situ hybridization (FISH) of a metaphase chromosomal spread. This technique uses polynucleotides as short as 500 or 600 bases; however, polynucleotides 2,000-4,000 bp are preferred. For a review of this technique, see Verma et al., “Human Chromosomes: a Manual of Basic Techniques,” Pergamon Press, New York (1988).

For chromosome mapping, the polynucleotides can be used individually (to mark a single chromosome or a single site on that chromosome) or in panels (for marking multiple sites and/or multiple chromosomes).

Thus, the present invention also provides a method for chromosomal localization which involves (a) preparing PCR primers from the polynucleotide sequences in Table 1B and/or Table 2 and SEQ ID NO:X and (b) screening somatic cell hybrids containing individual chromosomes.

The polynucleotides of the present invention would likewise be useful for radiation hybrid mapping, HAPPY mapping, and long range restriction mapping. For a review of these techniques and others known in the art, see, e.g. Dear, “Genome Mapping: A Practical Approach,” IRL Press at Oxford University Press, London (1997); Aydin, J. Mol. Med. 77:691-694 (1999); Hacia et al., Mol. Psychiatry. 3:483-492 (1998); Herrick et al., Chromosome Res. 7:409-423 (1999); Hamilton et al., Methods Cell Biol. 62:265-280 (2000); and/or Ott, J. Hered. 90:68-70 (1999) each of which is hereby incorporated by reference in its entirety.

Once a polynucleotide has been mapped to a precise chromosomal location, the physical position of the polynucleotide can be used in linkage analysis. Linkage analysis establishes coinheritance between a chromosomal location and presentation of a particular disease. (Disease mapping data are found, for example, in V. McKusick, Mendelian Inheritance in Man (available on line through Johns Hopkins University Welch Medical Library)). Column 9 of Table 1B.1 provides an OMIM reference identification number of diseases associated with the cytologic band disclosed in column 8 of Table 1B.1, as determined using techniques described herein and by reference to Table 5. Assuming 1 megabase mapping resolution and one gene per 20 kb, a cDNA precisely localized to a chromosomal region associated with the disease could be one of 50-500 potential causative genes.

Thus, once coinheritance is established, differences in a polynucleotide of the invention and the corresponding gene between affected and unaffected individuals can be examined. First, visible structural alterations in the chromosomes, such as deletions or translocations, are examined in chromosome spreads or by PCR. If no structural alterations exist, the presence of point mutations are ascertained. Mutations observed in some or all affected individuals, but not in normal individuals, indicates that the mutation may cause the disease. However, complete sequencing of the polypeptide and the corresponding gene from several normal individuals is required to distinguish the mutation from a polymorphism. If a new polymorphism is identified, this polymorphic polypeptide can be used for further linkage analysis.

Furthermore, increased or decreased expression of the gene in affected individuals as compared to unaffected individuals can be assessed using the polynucleotides of the invention. Any of these alterations (altered expression, chromosomal rearrangement, or mutation) can be used as a diagnostic or prognostic marker. Diagnostic and prognostic methods, kits and reagents encompassed by the present invention are briefly described below and more thoroughly elsewhere herein (see e.g., the sections labeled “Antibodies”, “Diagnostic Assays”, and “Methods for Detecting Diseases”).

Thus, the invention also provides a diagnostic method useful during diagnosis of a disorder, involving measuring the expression level of polynucleotides of the present invention in cells or body fluid from an individual and comparing the measured gene expression level with a standard level of polynucleotide expression level, whereby an increase or decrease in the gene expression level compared to the standard is indicative of a disorder. Additional non-limiting examples of diagnostic methods encompassed by the present invention are more thoroughly described elsewhere herein (see, e.g., Example 12).

In still another embodiment, the invention includes a kit for analyzing samples for the presence of proliferative and/or cancerous polynucleotides derived from a test subject. In a general embodiment, the kit includes at least one polynucleotide probe containing a nucleotide sequence that will specifically hybridize with a polynucleotide of the invention and a suitable container. In a specific embodiment, the kit includes two polynucleotide probes defining an internal region of the polynucleotide of the invention, where each probe has one strand containing a 31′mer-end internal to the region. In a further embodiment, the probes may be useful as primers for polymerase chain reaction amplification.

Where a diagnosis of a related disorder, including, for example, diagnosis of a tumor, has already been made according to conventional methods, the present invention is useful as a prognostic indicator, whereby patients exhibiting enhanced or depressed polynucleotide of the invention expression will experience a worse clinical outcome relative to patients expressing the gene at a level nearer the standard level.

By “measuring the expression level of polynucleotides of the invention” is intended qualitatively or quantitatively measuring or estimating the level of the polypeptide of the invention or the level of the mRNA encoding the polypeptide of the invention in a first biological sample either directly (e.g., by determining or estimating absolute protein level or mRNA level) or relatively (e.g., by comparing to the polypeptide level or mRNA level in a second biological sample). Preferably, the polypeptide level or mRNA level in the first biological sample is measured or estimated and compared to a standard polypeptide level or mRNA level, the standard being taken from a second biological sample obtained from an individual not having the related disorder or being determined by averaging levels from a population of individuals not having a related disorder. As will be appreciated in the art, once a standard polypeptide level or mRNA level is known, it can be used repeatedly as a standard for comparison.

By “biological sample” is intended any biological sample obtained from an individual, body fluid, cell line, tissue culture, or other source which contains polypeptide of the present invention or the corresponding mRNA. As indicated, biological samples include body fluids (such as semen, lymph, vaginal pool, sera, plasma, urine, synovial fluid and spinal fluid) which contain the polypeptide of the present invention, and tissue sources found to express the polypeptide of the present invention. Methods for obtaining tissue biopsies and body fluids from mammals are well known in the art. Where the biological sample is to include mRNA, a tissue biopsy is the preferred source.

The method(s) provided above may preferably be applied in a diagnostic method and/or kits in which polynucleotides and/or polypeptides of the invention are attached to a solid support. In one exemplary method, the support may be a “gene chip” or a “biological chip” as described in U.S. Pat. Nos. 5,837,832, 5,874,219, and 5,856,174. Further, such a gene chip with polynucleotides of the invention attached may be used to identify polymorphisms between the isolated polynucleotide sequences of the invention, with polynucleotides isolated from a test subject. The knowledge of such polymorphisms (i.e. their location, as well as, their existence) would be beneficial in identifying disease loci for many disorders, such as for example, in neural disorders, immune system disorders, muscular disorders, reproductive disorders, gastrointestinal disorders, pulmonary disorders, digestive disorders, metabolic disorders, cardiovascular disorders, renal disorders, proliferative disorders, and/or cancerous diseases and conditions. Such a method is described in U.S. Pat. Nos. 5,858,659 and 5,856,104. The U.S. patents referenced supra are hereby incorporated by reference in their entirety herein.

The present invention encompasses polynucleotides of the present invention that are chemically synthesized, or reproduced as peptide nucleic acids (PNA), or according to other methods known in the art. The use of PNAs would serve as the preferred form if the polynucleotides of the invention are incorporated onto a solid support, or gene chip. For the purposes of the present invention, a peptide nucleic acid (PNA) is a polyamide type of DNA analog and the monomeric units for adenine, guanine, thymine and cytosine are available commercially (Perceptive Biosystems). Certain components of DNA, such as phosphorus, phosphorus oxides, or deoxyribose derivatives, are not present in PNAs. As disclosed by Nielsen et al., Science 254, 1497 (1991); and Egholm et al., Nature 365, 666 (1993), PNAs bind specifically and tightly to complementary DNA strands and are not degraded by nucleases. In fact, PNA binds more strongly to DNA than DNA itself does. This is probably because there is no electrostatic repulsion between the two strands, and also the polyamide backbone is more flexible. Because of this, PNA/DNA duplexes bind under a wider range of stringency conditions than DNA/DNA duplexes, making it easier to perform multiplex hybridization. Smaller probes can be used than with DNA due to the strong binding. In addition, it is more likely that single base mismatches can be determined with PNA/DNA hybridization because a single mismatch in a PNA/DNA 15-mer lowers the melting point (T.sub.m) by 8°-20° C., vs. 4°-16° C. for the DNA/DNA 15-mer duplex. Also, the absence of charge groups in PNA means that hybridization can be done at low ionic strengths and reduce possible interference by salt during the analysis.

The compounds of the present invention have uses which include, but are not limited to, detecting cancer in mammals. In particular the invention is useful during diagnosis of pathological cell proliferative neoplasias which include, but are not limited to: acute myelogenous leukemias including acute monocytic leukemia, acute myeloblastic leukemia, acute promyelocytic leukemia, acute myelomonocytic leukemia, acute erythroleukemia, acute megakaryocytic leukemia, and acute undifferentiated leukemia, etc.; and chronic myelogenous leukemias including chronic myelomonocytic leukemia, chronic granulocytic leukemia, etc. Preferred mammals include monkeys, apes, cats, dogs, cows, pigs, horses, rabbits and humans. Particularly preferred are humans.

Pathological cell proliferative disorders are often associated with inappropriate activation of proto-oncogenes. (Gelmann, E. P. et al., “The Etiology of Acute Leukemia: Molecular Genetics and Viral Oncology,” in Neoplastic Diseases of the Blood, Vol 1., Wiernik, P. H. et al. eds., 161-182 (1985)). Neoplasias are now believed to result from the qualitative alteration of a normal cellular gene product, or from the quantitative modification of gene expression by insertion into the chromosome of a viral sequence, by chromosomal translocation of a gene to a more actively transcribed region, or by some other mechanism. (Gelmann et al., supra) It is likely that mutated or altered expression of specific genes is involved in the pathogenesis of some leukemias, among other tissues and cell types. (Gelmann et al., supra) Indeed, the human counterparts of the oncogenes involved in some animal neoplasias have been amplified or translocated in some cases of human leukemia and carcinoma. (Gelmann et al., supra)

For example, c-myc expression is highly amplified in the non-lymphocytic leukemia cell line HL-60. When HL-60 cells are chemically induced to stop proliferation, the level of c-myc is found to be downregulated. (International Publication Number WO 91/15580). However, it has been shown that exposure of HL-60 cells to a DNA construct that is complementary to the 5′ end of c-myc or c-myb blocks translation of the corresponding mRNAs which downregulates expression of the c-myc or c-myb proteins and causes arrest of cell proliferation and differentiation of the treated cells. (International Publication Number WO 91/15580; Wickstrom et al., Proc. Natl. Acad. Sci. 85:1028 (1988); Anfossi et al., Proc. Natl. Acad. Sci. 86:3379 (1989)). However, the skilled artisan would appreciate the present invention's usefulness is not be limited to treatment, prevention, and/or prognosis of proliferative disorders of cells and tissues of hematopoietic origin, in light of the numerous cells and cell types of varying origins which are known to exhibit proliferative phenotypes.

In addition to the foregoing, a polynucleotide of the present invention can be used to control gene expression through triple helix formation or through antisense DNA or RNA. Antisense techniques are discussed, for example, in Okano, J. Neurochem. 56: 560 (1991); “Oligodeoxynucleotides as Antisense Inhibitors of Gene Expression, CRC Press, Boca Raton, Fla. (1988). Triple helix formation is discussed in, for instance Lee et al., Nucleic Acids Research 6: 3073 (1979); Cooney et al., Science 241: 456 (1988); and Dervan et al., Science 251: 1360 (1991). Both methods rely on binding of the polynucleotide to a complementary DNA or RNA. For these techniques, preferred polynucleotides are usually oligonucleotides 20 to 40 bases in length and complementary to either the region of the gene involved in transcription (triple helix—see Lee et al., Nucl. Acids Res. 6:3073 (1979); Cooney et al., Science 241:456 (1988); and Dervan et al., Science 251:1360 (1991)) or to the mRNA itself (antisense—Okano, J. Neurochem. 56:560 (1991); Oligodeoxy-nucleotides as Antisense Inhibitors of Gene Expression, CRC Press, Boca Raton, Fla. (1988)). Triple helix formation optimally results in a shut-off of RNA transcription from DNA, while antisense RNA hybridization blocks translation of an mRNA molecule into polypeptide. The oligonucleotide described above can also be delivered to cells such that the antisense RNA or DNA may be expressed in vivo to inhibit production of polypeptide of the present invention antigens. Both techniques are effective in model systems, and the information disclosed herein can be used to design antisense or triple helix polynucleotides in an effort to treat disease, and in particular, for the treatment of proliferative diseases and/or conditions. Non-limiting antisense and triple helix methods encompassed by the present invention are more thoroughly described elsewhere herein (see, e.g., the section labeled “Antisense and Ribozyme (Antagonists)”).

Polynucleotides of the present invention are also useful in gene therapy. One goal of gene therapy is to insert a normal gene into an organism having a defective gene, in an effort to correct the genetic defect. The polynucleotides disclosed in the present invention offer a means of targeting such genetic defects in a highly accurate manner. Another goal is to insert a new gene that was not present in the host genome, thereby producing a new trait in the host cell. Additional non-limiting examples of gene therapy methods encompassed by the present invention are more thoroughly described elsewhere herein (see, e.g., the sections labeled “Gene Therapy Methods”, and Examples 16, 17 and 18).

The polynucleotides are also useful for identifying individuals from minute biological samples. The United States military, for example, is considering the use of restriction fragment length polymorphism (RFLP) for identification of its personnel. In this technique, an individual's genomic DNA is digested with one or more restriction enzymes, and probed on a Southern blot to yield unique bands for identifying personnel. This method does not suffer from the current limitations of “Dog Tags” which can be lost, switched, or stolen, making positive identification difficult. The polynucleotides of the present invention can be used as additional DNA markers for RFLP.

The polynucleotides of the present invention can also be used as an alternative to RFLP, by determining the actual base-by-base DNA sequence of selected portions of an individual's genome. These sequences can be used to prepare PCR primers for amplifying and isolating such selected DNA, which can then be sequenced. Using this technique, individuals can be identified because each individual will have a unique set of DNA sequences. Once an unique ID database is established for an individual, positive identification of that individual, living or dead, can be made from extremely small tissue samples.

Forensic biology also benefits from using DNA-based identification techniques as disclosed herein. DNA sequences taken from very small biological samples such as tissues, e.g., hair or skin, or body fluids, e.g., blood, saliva, semen, synovial fluid, amniotic fluid, breast milk, lymph, pulmonary sputum or surfactant, urine, fecal matter, etc., can be amplified using PCR. In one prior art technique, gene sequences amplified from polymorphic loci, such as DQa class II HLA gene, are used in forensic biology to identify individuals. (Erlich, H., PCR Technology, Freeman and Co. (1992)). Once these specific polymorphic loci are amplified, they are digested with one or more restriction enzymes, yielding an identifying set of bands on a Southern blot probed with DNA corresponding to the DQa class II HLA gene. Similarly, polynucleotides of the present invention can be used as polymorphic markers for forensic purposes.

There is also a need for reagents capable of identifying the source of a particular tissue. Such need arises, for example, in forensics when presented with tissue of unknown origin. Appropriate reagents can comprise, for example, DNA probes or primers prepared from the sequences of the present invention, specific to tissues, including but not limited to those shown in Table 1B. Panels of such reagents can identify tissue by species and/or by organ type. In a similar fashion, these reagents can be used to screen tissue cultures for contamination. Additional non-limiting examples of such uses are further described herein.

The polynucleotides of the present invention are also useful as hybridization probes for differential identification of the tissue(s) or cell type(s) present in a biological sample. Similarly, polypeptides and antibodies directed to polypeptides of the present invention are useful to provide immunological probes for differential identification of the tissue(s) (e.g., immunohistochemistry assays) or cell type(s) (e.g., immunocytochemistry assays). In addition, for a number of disorders of the above tissues or cells, significantly higher or lower levels of gene expression of the polynucleotides/polypeptides of the present invention may be detected in certain tissues (e.g., tissues expressing polypeptides and/or polynucleotides of the present invention, for example, those disclosed in Table 1B, and/or cancerous and/or wounded tissues) or bodily fluids (e.g., semen, lymph, vaginal pool, serum, plasma, urine, synovial fluid or spinal fluid) taken from an individual having such a disorder, relative to a “standard” gene expression level, i.e., the expression level in healthy tissue from an individual not having the disorder.

Thus, the invention provides a diagnostic method of a disorder, which involves: (a) assaying gene expression level in cells or body fluid of an individual; (b) comparing the gene expression level with a standard gene expression level, whereby an increase or decrease in the assayed gene expression level compared to the standard expression level is indicative of a disorder.

In the very least, the polynucleotides of the present invention can be used as molecular weight markers on Southern gels, as diagnostic probes for the presence of a specific mRNA in a particular cell type, as a probe to “subtract-out” known sequences in the process of discovering novel polynucleotides, for selecting and making oligomers for attachment to a “gene chip” or other support, to raise anti-DNA antibodies using DNA immunization techniques, and as an antigen to elicit an immune response.

Uses of the Polypeptides

Each of the polypeptides identified herein can be used in numerous ways. The following description should be considered exemplary and utilizes known techniques.

Polypeptides and antibodies directed to polypeptides of the present invention are useful to provide immunological probes for differential identification of the tissue(s) (e.g., immunohistochemistry assays such as, for example, ABC immunoperoxidase (Hsu et al., J. Histochem. Cytochem. 29:577-580 (1981)) or cell type(s) (e.g., immunocytochemistry assays).

Antibodies can be used to assay levels of polypeptides encoded by polynucleotides of the invention in a biological sample using classical immunohistological methods known to those of skill in the art (e.g., see Jalkanen, et al., J. Cell. Biol. 101:976-985 (1985); Jalkanen, et al., J. Cell. Biol. 105:3087-3096 (1987)). Other antibody-based methods useful for detecting protein gene expression include immunoassays, such as the enzyme linked immunosorbent assay (ELISA) and the radioimmunoassay (RIA). Suitable antibody assay labels are known in the art and include enzyme labels, such as, glucose oxidase; radioisotopes, such as iodine (¹³¹I, ¹²⁵I, ¹²³I, ¹²¹I), carbon (¹⁴C), sulfur (³⁵S), tritium (³H), indium (^(115m)In, ^(113m)In, ¹¹²In, ¹¹¹In), and technetium (⁹⁹Tc, ^(99m)Tc), thallium (²⁰¹Ti), gallium (⁶⁸Ga, ⁶⁷Ga), palladium (¹⁰³Pd), molybdenum (⁹⁹Mo), xenon (¹³³Xe), fluorine (¹⁸F), ¹⁵³Sm, ¹⁷⁷Lu, ¹⁵⁹Gd, ¹⁴⁹Pm, ¹⁴⁰La, ¹⁷⁵Yb, ¹⁶⁶Ho, ⁹⁰Y, ⁴⁷Sc, ¹⁸⁶Re, Re, ¹⁴²Pr, ¹⁰⁵Rh, ⁹⁷Ru; luminescent labels, such as luminol; and fluorescent labels, such as fluorescein and rhodamine, and biotin.

In addition to assaying levels of polypeptide of the present invention in a biological sample, proteins can also be detected in vivo by imaging. Antibody labels or markers for in vivo imaging of protein include those detectable by X-radiography, NMR or ESR. For X-radiography, suitable labels include radioisotopes such as barium or cesium, which emit detectable radiation but are not overtly harmful to the subject. Suitable markers for NMR and ESR include those with a detectable characteristic spin, such as deuterium, which may be incorporated into the antibody by labeling of nutrients for the relevant hybridoma.

A protein-specific antibody or antibody fragment which has been labeled with an appropriate detectable imaging moiety, such as a radioisotope (for example, ¹³¹I, ¹¹²In, ^(99m)Tc, (¹³¹I, ¹²⁵I, ¹²³I, ¹²¹I), carbon (¹⁴C), sulfur (³⁵S), tritium (³H), indium (^(115m)In, ^(113m)In, ¹¹²In, ¹¹¹In), and technetium (⁹⁹Tc, ^(99m)Tc), thallium (²⁰¹Ti), gallium (⁶⁸Ga, ⁶⁷Ga), palladium (¹⁰³Pd), molybdenum (⁹⁹Mo), xenon (¹³³Xe), fluorine (¹⁸F, ¹⁵³Sm, ¹⁷⁷Lu, ¹⁵⁹Gd, ¹⁴⁹Pm, ¹⁴⁰La, ¹⁷⁵Yb, ¹⁶⁶Ho, ⁹⁰Y, ⁴⁷Sc, ¹⁸⁶Re, ¹⁸⁸Re, ¹⁴²Pr, ¹⁰⁵Rh, ⁹⁷Ru), a radio-opaque substance, or a material detectable by nuclear magnetic resonance, is introduced (for example, parenterally, subcutaneously or intraperitoneally) into the mammal to be examined for immune system disorder. It will be understood in the art that the size of the subject and the imaging system used will determine the quantity of imaging moiety needed to produce diagnostic images. In the case of a radioisotope moiety, for a human subject, the quantity of radioactivity injected will normally range from about 5 to 20 millicuries of ^(99m)Tc. The labeled antibody or antibody fragment will then preferentially accumulate at the location of cells which express the polypeptide encoded by a polynucleotide of the invention. In vivo tumor imaging is described in S. W. Burchiel et al., “Immunopharmacokinetics of Radiolabeled Antibodies and Their Fragments” (Chapter 13 in Tumor Imaging: The Radiochemical Detection of Cancer, S. W. Burchiel and B. A. Rhodes, eds., Masson Publishing Inc. (1982)).

In one embodiment, the invention provides a method for the specific delivery of compositions of the invention to cells by administering polypeptides of the invention (e.g., polypeptides encoded by polynucleotides of the invention and/or antibodies) that are associated with heterologous polypeptides or nucleic acids. In one example, the invention provides a method for delivering a therapeutic protein into the targeted cell. In another example, the invention provides a method for delivering a single stranded nucleic acid (e.g., antisense or ribozymes) or double stranded nucleic acid (e.g., DNA that can integrate into the cell's genome or replicate episomally and that can be transcribed) into the targeted cell.

In another embodiment, the invention provides a method for the specific destruction of cells (e.g., the destruction of tumor cells) by administering polypeptides of the invention in association with toxins or cytotoxic prodrugs.

By “toxin” is meant one or more compounds that bind and activate endogenous cytotoxic effector systems, radioisotopes, holotoxins, modified toxins, catalytic subunits of toxins, or any molecules or enzymes not normally present in or on the surface of a cell that under defined conditions cause the cell's death. Toxins that may be used according to the methods of the invention include, but are not limited to, radioisotopes known in the art, compounds such as, for example, antibodies (or complement fixing containing portions thereof) that bind an inherent or induced endogenous cytotoxic effector system, thymidine kinase, endonuclease, RNAse, alpha toxin, ricin, abrin, Pseudomonas exotoxin A, diphtheria toxin, saporin, momordin, gelonin, pokeweed antiviral protein, alpha-sarcin and cholera toxin. “Toxin” also includes a cytostatic or cytocidal agent, a therapeutic agent or a radioactive metal ion, e.g., alpha-emitters such as, for example, ²¹³Bi, or other radioisotopes such as, for example, ¹⁰³Pd, ¹³³Xe, 1311,68Ge, ⁵⁷Co, ⁶⁵Zn, ⁸⁵Sr, ³²P, ³⁵S, ⁹⁰Y, ¹⁵³Sm, ¹⁵³Gd, ¹⁶⁹Yb, ⁵Cr, ⁵⁴Mn, ⁷⁵Se, ¹¹³Sn, ⁹⁰Yttrium, ¹¹⁷Tin, ¹⁸⁶Rhenium, ¹⁶⁶Holmium, and ¹⁸⁸Rhenium; luminescent labels, such as luminol; and fluorescent labels, such as fluorescein and rhodamine, and biotin. In a specific embodiment, the invention provides a method for the specific destruction of cells (e.g., the destruction of tumor cells) by administering polypeptides of the invention or antibodies of the invention in association with the radioisotope ⁹⁰Y. In another specific embodiment, the invention provides a method for the specific destruction of cells (e.g., the destruction of tumor cells) by administering polypeptides of the invention or antibodies of the invention in association with the radioisotope ¹¹¹In. In a further specific embodiment, the invention provides a method for the specific destruction of cells (e.g., the destruction of tumor cells) by administering polypeptides of the invention or antibodies of the invention in association with the radioisotope ¹³¹I.

Techniques known in the art may be applied to label polypeptides of the invention (including antibodies). Such techniques include, but are not limited to, the use of bifunctional conjugating agents (see e.g., U.S. Pat. Nos. 5,756,065; 5,714,631; 5,696,239; 5,652,361; 5,505,931; 5,489,425; 5,435,990; 5,428,139; 5,342,604; 5,274,119; 4,994,560; and 5,808,003; the contents of each of which are hereby incorporated by reference in its entirety).

Thus, the invention provides a diagnostic method of a disorder, which involves (a) assaying the expression level of a polypeptide of the present invention in cells or body fluid of an individual; and (b) comparing the assayed polypeptide expression level with a standard polypeptide expression level, whereby an increase or decrease in the assayed polypeptide expression level compared to the standard expression level is indicative of a disorder. With respect to cancer, the presence of a relatively high amount of transcript in biopsied tissue from an individual may indicate a predisposition for the development of the disease, or may provide a means for detecting the disease prior to the appearance of actual clinical symptoms. A more definitive diagnosis of this type may allow health professionals to employ preventative measures or aggressive treatment earlier thereby preventing the development or further progression of the cancer.

Moreover, polypeptides of the present invention can be used to treat or prevent diseases or conditions such as, for example, neural disorders, immune system disorders, muscular disorders, reproductive disorders, gastrointestinal disorders, pulmonary disorders, cardiovascular disorders, renal disorders, proliferative disorders, and/or cancerous diseases and conditions. For example, patients can be administered a polypeptide of the present invention in an effort to replace absent or decreased levels of the polypeptide (e.g., insulin), to supplement absent or decreased levels of a different polypeptide (e.g., hemoglobin S for hemoglobin B, SOD, catalase, DNA repair proteins), to inhibit the activity of a polypeptide (e.g., an oncogene or tumor supressor), to activate the activity of a polypeptide (e.g., by binding to a receptor), to reduce the activity of a membrane bound receptor by competing with it for free ligand (e.g., soluble TNF receptors used in reducing inflammation), or to bring about a desired response (e.g., blood vessel growth inhibition, enhancement of the immune response to proliferative cells or tissues).

Similarly, antibodies directed to a polypeptide of the present invention can also be used to treat disease (as described supra, and elsewhere herein). For example, administration of an antibody directed to a polypeptide of the present invention can bind, and/or neutralize the polypeptide, and/or reduce overproduction of the polypeptide. Similarly, administration of an antibody can activate the polypeptide, such as by binding to a polypeptide bound to a membrane (receptor).

At the very least, the polypeptides of the present invention can be used as molecular weight markers on SDS-PAGE gels or on molecular sieve gel filtration columns using methods well known to those of skill in the art. Polypeptides can also be used to raise antibodies, which in turn are used to measure protein expression from a recombinant cell, as a way of assessing transformation of the host cell. Moreover, the polypeptides of the present invention can be used to test the biological activities described herein.

Diagnostic Assays

The compounds of the present invention are useful for diagnosis, treatment, prevention and/or prognosis of various disorders in mammals, preferably humans. Such disorders include, but are not limited to, those related to biological activities described in Table 1D and, also as described herein under the section heading “Biological Activities”.

For a number of disorders, substantially altered (increased or decreased) levels of gene expression can be detected in tissues, cells or bodily fluids (e.g., sera, plasma, urine, semen, synovial fluid or spinal fluid) taken from an individual having such a disorder, relative to a “standard” gene expression level, that is, the expression level in tissues or bodily fluids from an individual not having the disorder. Thus, the invention provides a diagnostic method useful during diagnosis of a disorder, which involves measuring the expression level of the gene encoding the polypeptide in tissues, cells or body fluid from an individual and comparing the measured gene expression level with a standard gene expression level, whereby an increase or decrease in the gene expression level(s) compared to the standard is indicative of a disorder. These diagnostic assays may be performed in vivo or in vitro, such as, for example, on blood samples, biopsy tissue or autopsy tissue.

The present invention is also useful as a prognostic indicator, whereby patients exhibiting enhanced or depressed gene expression will experience a worse clinical outcome relative to patients expressing the gene at a level nearer the standard level.

In certain embodiments, a polypeptide of the invention, or polynucleotides, antibodies, agonists, or antagonists corresponding to that polypeptide, may be used to diagnose and/or prognosticate diseases and/or disorders associated with the tissue(s) in which the polypeptide of the invention is expressed, including one, two, three, four, five, or more tissues disclosed in Table 1B.2, column 5 (Tissue Distribution Library Code).

By “assaying the expression level of the gene encoding the polypeptide” is intended qualitatively or quantitatively measuring or estimating the level of the polypeptide of the invention or the level of the mRNA encoding the polypeptide of the invention in a first biological sample either directly (e.g., by determining or estimating absolute protein level or mRNA level) or relatively (e.g., by comparing to the polypeptide level or mRNA level in a second biological sample). Preferably, the polypeptide expression level or mRNA level in the first biological sample is measured or estimated and compared to a standard polypeptide level or mRNA level, the standard being taken from a second biological sample obtained from an individual not having the disorder or being determined by averaging levels from a population of individuals not having the disorder. As will be appreciated in the art, once a standard polypeptide level or mRNA level is known, it can be used repeatedly as a standard for comparison.

By “biological sample” is intended any biological sample obtained from an individual, cell line, tissue culture, or other source containing polypeptides of the invention (including portions thereof) or mRNA. As indicated, biological samples include body fluids (such as sera, plasma, urine, synovial fluid and spinal fluid) and tissue sources found to express the full length or fragments thereof of a polypeptide or mRNA. Methods for obtaining tissue biopsies and body fluids from mammals are well known in the art. Where the biological sample is to include mRNA, a tissue biopsy is the preferred source.

Total cellular RNA can be isolated from a biological sample using any suitable technique such as the single-step guanidinium-thiocyanate-phenol-chloroform method described in Chomczynski and Sacchi, Anal. Biochem. 162:156-159 (1987). Levels of mRNA encoding the polypeptides of the invention are then assayed using any appropriate method. These include Northern blot analysis, S1 nuclease mapping, the polymerase chain reaction (PCR), reverse transcription in combination with the polymerase chain reaction (RT-PCR), and reverse transcription in combination with the ligase chain reaction (RT-LCR).

The present invention also relates to diagnostic assays such as quantitative and diagnostic assays for detecting levels of polypeptides of the invention, in a biological sample (e.g., cells and tissues), including determination of normal and abnormal levels of polypeptides. Thus, for instance, a diagnostic assay in accordance with the invention for detecting over-expression of polypeptides of the invention compared to normal control tissue samples may be used to detect the presence of tumors. Assay techniques that can be used to determine levels of a polypeptide, such as a polypeptide of the present invention in a sample derived from a host are well-known to those of skill in the art. Such assay methods include radioimmunoassays, competitive-binding assays, Western Blot analysis and ELISA assays. Assaying polypeptide levels in a biological sample can occur using any art-known method.

Assaying polypeptide levels in a biological sample can occur using antibody-based techniques. For example, polypeptide expression in tissues can be studied with classical immunohistological methods (Jalkanen et al., J. Cell. Biol. 101:976-985 (1985); Jalkanen, M., et al., J. Cell. Biol. 105:3087-3096 (1987)). Other antibody-based methods useful for detecting polypeptide gene expression include immunoassays, such as the enzyme linked immunosorbent assay (ELISA) and the radioimmunoassay (RIA). Suitable antibody assay labels are known in the art and include enzyme labels, such as, glucose oxidase, and radioisotopes, such as iodine (¹²⁵I, ¹²¹I), carbon (¹⁴C), sulfur (³⁵S), tritium (³H), indium (¹¹²In), and technetium (^(99m)Tc), and fluorescent labels, such as fluorescein and rhodamine, and biotin.

The tissue or cell type to be analyzed will generally include those which are known, or suspected, to express the gene of interest (such as, for example, cancer). The protein isolation methods employed herein may, for example, be such as those described in Harlow and Lane (Harlow, E. and Lane, D., 1988, “Antibodies: A Laboratory Manual”, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y.), which is incorporated herein by reference in its entirety. The isolated cells can be derived from cell culture or from a patient. The analysis of cells taken from culture may be a necessary step in the assessment of cells that could be used as part of a cell-based gene therapy technique or, alternatively, to test the effect of compounds on the expression of the gene.

For example, antibodies, or fragments of antibodies, such as those described herein, may be used to quantitatively or qualitatively detect the presence of gene products or conserved variants or peptide fragments thereof. This can be accomplished, for example, by immunofluorescence techniques employing a fluorescently labeled antibody coupled with light microscopic, flow cytometric, or fluorimetric detection.

In a preferred embodiment, antibodies, or fragments of antibodies directed to any one or all of the predicted epitope domains of the polypeptides of the invention (shown in column 7 of Table 1B.1) may be used to quantitatively or qualitatively detect the presence of gene products or conserved variants or peptide fragments thereof. This can be accomplished, for example, by immunofluorescence techniques employing a fluorescently labeled antibody coupled with light microscopic, flow cytometric, or fluorimetric detection.

In an additional preferred embodiment, antibodies, or fragments of antibodies directed to a conformational epitope of a polypeptide of the invention may be used to quantitatively or qualitatively detect the presence of gene products or conserved variants or peptide fragments thereof. This can be accomplished, for example, by immunofluorescence techniques employing a fluorescently labeled antibody coupled with light microscopic, flow cytometric, or fluorimetric detection.

The antibodies (or fragments thereof), and/or polypeptides of the present invention may, additionally, be employed histologically, as in immunofluorescence, immunoelectron microscopy or non-immunological assays, for in situ detection of gene products or conserved variants or peptide fragments thereof. In situ detection may be accomplished by removing a histological specimen from a patient, and applying thereto a labeled antibody or polypeptide of the present invention. The antibody (or fragment thereof) or polypeptide is preferably applied by overlaying the labeled antibody (or fragment) onto a biological sample. Through the use of such a procedure, it is possible to determine not only the presence of the gene product, or conserved variants or peptide fragments, or polypeptide binding, but also its distribution in the examined tissue. Using the present invention, those of ordinary skill will readily perceive that any of a wide variety of histological methods (such as staining procedures) can be modified in order to achieve such in situ detection.

Immunoassays and non-immunoassays for gene products or conserved variants or peptide fragments thereof will typically comprise incubating a sample, such as a biological fluid, a tissue extract, freshly harvested cells, or lysates of cells which have been incubated in cell culture, in the presence of a detectably labeled antibody capable of binding gene products or conserved variants or peptide fragments thereof, and detecting the bound antibody by any of a number of techniques well-known in the art.

The biological sample may be brought in contact with and immobilized onto a solid phase support or carrier such as nitrocellulose, or other solid support which is capable of immobilizing cells, cell particles or soluble proteins. The support may then be washed with suitable buffers followed by treatment with the detectably labeled antibody or detectable polypeptide of the invention. The solid phase support may then be washed with the buffer a second time to remove unbound antibody or polypeptide. Optionally the antibody is subsequently labeled. The amount of bound label on solid support may then be detected by conventional means.

By “solid phase support or carrier” is intended any support capable of binding an antigen or an antibody. Well-known supports or carriers include glass, polystyrene, polypropylene, polyethylene, dextran, nylon, amylases, natural and modified celluloses, polyacrylamides, gabbros, and magnetite. The nature of the carrier can be either soluble to some extent or insoluble for the purposes of the present invention. The support material may have virtually any possible structural configuration so long as the coupled molecule is capable of binding to an antigen or antibody. Thus, the support configuration may be spherical, as in a bead, or cylindrical, as in the inside surface of a test tube, or the external surface of a rod. Alternatively, the surface may be flat such as a sheet, test strip, etc. Preferred supports include polystyrene beads. Those skilled in the art will know many other suitable carriers for binding antibody or antigen, or will be able to ascertain the same by use of routine experimentation.

The binding activity of a given lot of antibody or antigen polypeptide may be determined according to well known methods. Those skilled in the art will be able to determine operative and optimal assay conditions for each determination by employing routine experimentation.

In addition to assaying polypeptide levels or polynucleotide levels in a biological sample obtained from an individual, polypeptide or polynucleotide can also be detected in vivo by imaging. For example, in one embodiment of the invention, polypeptides and/or antibodies of the invention are used to image diseased cells, such as neoplasms. In another embodiment, polynucleotides of the invention (e.g., polynucleotides complementary to all or a portion of an mRNA) and/or antibodies (e.g., antibodies directed to any one or a combination of the epitopes of a polypeptide of the invention, antibodies directed to a conformational epitope of a polypeptide of the invention, or antibodies directed to the full length polypeptide expressed on the cell surface of a mammalian cell) are used to image diseased or neoplastic cells.

Antibody labels or markers for in vivo imaging of polypeptides of the invention include those detectable by X-radiography, NMR, MRI, CAT-scans or ESR. For X-radiography, suitable labels include radioisotopes such as barium or cesium, which emit detectable radiation but are not overtly harmful to the subject. Suitable markers for NMR and ESR include those with a detectable characteristic spin, such as deuterium, which may be incorporated into the antibody by labeling of nutrients for the relevant hybridoma. Where in vivo imaging is used to detect enhanced levels of polypeptides for diagnosis in humans, it may be preferable to use human antibodies or “humanized” chimeric monoclonal antibodies. Such antibodies can be produced using techniques described herein or otherwise known in the art. For example methods for producing chimeric antibodies are known in the art. See, for review, Morrison, Science 229:1202 (1985); Oi et al., BioTechniques 4:214 (1986); Cabilly et al., U.S. Pat. No. 4,816,567; Taniguchi et al., EP 171496; Morrison et al., EP 173494; Neuberger et al., WO 8601533; Robinson et al., WO 8702671; Boulianne et al., Nature 312:643 (1984); Neuberger et al., Nature 314:268 (1985).

Additionally, any polypeptides of the invention whose presence can be detected, can be administered. For example, polypeptides of the invention labeled with a radio-opaque or other appropriate compound can be administered and visualized in vivo, as discussed, above for labeled antibodies. Further, such polypeptides can be utilized for in vitro diagnostic procedures.

A polypeptide-specific antibody or antibody fragment which has been labeled with an appropriate detectable imaging moiety, such as a radioisotope (for example, ¹³¹I, ¹¹²In, ^(99m)Tc), a radio-opaque substance, or a material detectable by nuclear magnetic resonance, is introduced (for example, parenterally, subcutaneously or intraperitoneally) into the mammal to be examined for a disorder. It will be understood in the art that the size of the subject and the imaging system used will determine the quantity of imaging moiety needed to produce diagnostic images. In the case of a radioisotope moiety, for a human subject, the quantity of radioactivity injected will normally range from about 5 to 20 millicuries of ^(99m)Tc. The labeled antibody or antibody fragment will then preferentially accumulate at the location of cells which contain the antigenic protein. In vivo tumor imaging is described in S. W. Burchiel et al., “Immunopharmacokinetics of Radiolabeled Antibodies and Their Fragments” (Chapter 13 in Tumor Imaging: The Radiochemical Detection of Cancer, S. W. Burchiel and B. A. Rhodes, eds., Masson Publishing Inc. (1982)).

With respect to antibodies, one of the ways in which an antibody of the present invention can be detectably labeled is by linking the same to a reporter enzyme and using the linked product in an enzyme immunoassay (EIA) (Voller, A., “The Enzyme Linked Immunosorbent Assay (ELISA)”, 1978, Diagnostic Horizons 2:1-7, Microbiological Associates Quarterly Publication, Walkersville, Md.); Voller et al., J. Clin. Pathol. 31:507-520 (1978); Butler, J. E., Meth. Enzymol. 73:482-523 (1981); Maggio, E. (ed.), 1980, Enzyme Immunoassay, CRC Press, Boca Raton, Fla.,; Ishikawa, E. et al., (eds.), 1981, Enzyme Immunoassay, Kgaku Shoin, Tokyo). The reporter enzyme which is bound to the antibody will react with an appropriate substrate, preferably a chromogenic substrate, in such a manner as to produce a chemical moiety which can be detected, for example, by spectrophotometric, fluorimetric or by visual means. Reporter enzymes which can be used to detectably label the antibody include, but are not limited to, malate dehydrogenase, staphylococcal nuclease, delta-5-steroid isomerase, yeast alcohol dehydrogenase, alpha-glycerophosphate, dehydrogenase, triose phosphate isomerase, horseradish peroxidase, alkaline phosphatase, asparaginase, glucose oxidase, beta-galactosidase, ribonuclease, urease, catalase, glucose-6-phosphate dehydrogenase, glucoamylase and acetylcholinesterase. Additionally, the detection can be accomplished by colorimetric methods which employ a chromogenic substrate for the reporter enzyme. Detection may also be accomplished by visual comparison of the extent of enzymatic reaction of a substrate in comparison with similarly prepared standards.

Detection may also be accomplished using any of a variety of other immunoassays. For example, by radioactively labeling the antibodies or antibody fragments, it is possible to detect polypeptides through the use of a radioimmunoassay (RIA) (see, for example, Weintraub, B., Principles of Radioimmunoassays, Seventh Training Course on Radioligand Assay Techniques, The Endocrine Society, March, 1986, which is incorporated by reference herein). The radioactive isotope can be detected by means including, but not limited to, a gamma counter, a scintillation counter, or autoradiography.

It is also possible to label the antibody with a fluorescent compound. When the fluorescently labeled antibody is exposed to light of the proper wave length, its presence can then be detected due to fluorescence. Among the most commonly used fluorescent labeling compounds are fluorescein isothiocyanate, rhodamine, phycoerythrin, phycocyanin, allophycocyanin, ophthaldehyde and fluorescamine.

The antibody can also be detectably labeled using fluorescence emitting metals such as ¹⁵²Eu, or others of the lanthanide series. These metals can be attached to the antibody using such metal chelating groups as diethylenetriaminepentacetic acid (DTPA) or ethylenediaminetetraacetic acid (EDTA).

The antibody also can be detectably labeled by coupling it to a chemiluminescent compound. The presence of the chemiluminescent-tagged antibody is then determined by detecting the presence of luminescence that arises during the course of a chemical reaction. Examples of particularly useful chemiluminescent labeling compounds are luminol, isoluminol, theromatic acridinium ester, imidazole, acridinium salt and oxalate ester.

Likewise, a bioluminescent compound may be used to label the antibody of the present invention. Bioluminescence is a type of chemiluminescence found in biological systems in, which a catalytic protein increases the efficiency of the chemiluminescent reaction. The presence of a bioluminescent protein is determined by detecting the presence of luminescence. Important bioluminescent compounds for purposes of labeling are luciferin, luciferase and aequorin.

Methods for Detecting Diseases

In general, a disease may be detected in a patient based on the presence of one or more proteins of the invention and/or polynucleotides encoding such proteins in a biological sample (for example, blood, sera, urine, and/or tumor biopsies) obtained from the patient. In other words, such proteins may be used as markers to indicate the presence or absence of a disease or disorder, including cancer and/or as described elsewhere herein. In addition, such proteins may be useful for the detection of other diseases and cancers. The binding agents provided herein generally permit detection of the level of antigen that binds to the agent in the biological sample. Polynucleotide primers and probes may be used to detect the level of mRNA encoding polypeptides of the invention, which is also indicative of the presence or absence of a disease or disorder, including cancer. In general, polypeptides of the invention should be present at a level that is at least three fold higher in diseased tissue than in normal tissue.

There are a variety of assay formats known to those of ordinary skill in the art for using a binding agent to detect polypeptide markers in a sample. See, e.g., Harlow and Lane, supra. In general, the presence or absence of a disease in a patient may be determined by (a) contacting a biological sample obtained from a patient with a binding agent; (b) detecting in the sample a level of polypeptide that binds to the binding agent; and (c) comparing the level of polypeptide with a predetermined cut-off value.

In a preferred embodiment, the assay involves the use of a binding agent(s) immobilized on a solid support to bind to and remove the polypeptide of the invention from the remainder of the sample. The bound polypeptide may then be detected using a detection reagent that contains a reporter group and specifically binds to the binding agent/polypeptide complex. Such detection reagents may comprise, for example, a binding agent that specifically binds to the polypeptide or an antibody or other agent that specifically binds to the binding agent, such as an anti-immunoglobulin, protein G, protein A or a lectin. Alternatively, a competitive assay may be utilized, in which a polypeptide is labeled with a reporter group and allowed to bind to the immobilized binding agent after incubation of the binding agent with the sample. The extent to which components of the sample inhibit the binding of the labeled polypeptide to the binding agent is indicative of the reactivity of the sample with the immobilized binding agent. Suitable polypeptides for use within such assays include polypeptides of the invention and portions thereof, or antibodies, to which the binding agent binds, as described above.

The solid support may be any material known to those of skill in the art to which polypeptides of the invention may be attached. For example, the solid support may be a test well in a microtiter plate or a nitrocellulose or other suitable membrane. Alternatively, the support may be a bead or disc, such as glass fiberglass, latex or a plastic material such as polystyrene or polyvinylchloride. The support may also be a magnetic particle or a fiber optic sensor, such as those disclosed, for example, in U.S. Pat. No. 5,359,681. The binding agent may be immobilized on the solid support using a variety of techniques known to those of skill in the art, which are amply described in the patent and scientific literature. In the context of the present invention, the term “immobilization” refers to both noncovalent association, such as adsorption, and covalent attachment (which may be a direct linkage between the agent and functional groups on the support or may be a linkage by way of a cross-linking agent). Immobilization by adsorption to a well in a microtiter plate or to a membrane is preferred. In such cases, adsorption may be achieved by contacting the binding agent, in a suitable buffer, with the solid support for the suitable amount of time. The contact time varies with temperature, but is typically between about 1 hour and about 1 day. In general, contacting a well of plastic microtiter plate (such as polystyrene or polyvinylchloride) with an amount of binding agent ranging from about 10 ng to about 10 ug, and preferably about 100 ng to about 1 ug, is sufficient to immobilize an adequate amount of binding agent.

Covalent attachment of binding agent to a solid support may generally be achieved by first reacting the support with a bifunctional reagent that will react with both the support and a functional group, such as a hydroxyl or amino group, on the binding agent. For example, the binding agent may be covalently attached to supports having an appropriate polymer coating using benzoquinone or by condensation of an aldehyde group on the support with an amine and an active hydrogen on the binding partner (see, e.g., Pierce Immunotechnology Catalog and Handbook, 1991, at A12-A13).

Gene Therapy Methods

Also encompassed by the invention are gene therapy methods for treating or preventing disorders, diseases and conditions. The gene therapy methods relate to the introduction of nucleic acid (DNA, RNA and antisense DNA or RNA) sequences into an animal to achieve expression of the polypeptide of the present invention. This method requires a polynucleotide which codes for a polypeptide of the present invention operatively linked to a promoter and any other genetic elements necessary for the expression of the polypeptide by the target tissue. Such gene therapy and delivery techniques are known in the art, see, for example, WO90/11092, which is herein incorporated by reference.

Thus, for example, cells from a patient may be engineered with a polynucleotide (DNA or RNA) comprising a promoter operably linked to a polynucleotide of the present invention ex vivo, with the engineered cells then being provided to a patient to be treated with the polypeptide of the present invention. Such methods are well-known in the art. For example, see Belldegrun, A., et al., J. Natl. Cancer Inst. 85: 207-216 (1993); Ferrantini, M. et al., Cancer Research 53: 1107-1112 (1993); Ferrantini, M. et al., J. Immunology 153: 4604-4615 (1994); Kaido, T., et al., Int. J. Cancer 60: 221-229 (1995); Ogura, H., et al., Cancer Research 50: 5102-5106 (1990); Santodonato, L., et al., Human Gene Therapy 7:1-10 (1996); Santodonato, L., et al., Gene Therapy 4:1246-1255 (1997); and Zhang, J.-F. et al., Cancer Gene Therapy 3: 31-38 (1996)), which are herein incorporated by reference. In one embodiment, the cells which are engineered are arterial cells. The arterial cells may be reintroduced into the patient through direct injection to the artery, the tissues surrounding the artery, or through catheter injection.

As discussed in more detail below, the polynucleotide constructs can be delivered by any method that delivers injectable materials to the cells of an animal, such as, injection into the interstitial space of tissues (heart, muscle, skin, lung, liver, and the like). The polynucleotide constructs may be delivered in a pharmaceutically acceptable liquid or aqueous carrier.

In one embodiment, the polynucleotide of the present invention is delivered as a naked polynucleotide. The term “naked” polynucleotide, DNA or RNA refers to sequences that are free from any delivery vehicle that acts to assist, promote or facilitate entry into the cell, including viral sequences, viral particles, liposome formulations, LIPOFECTIN™ or precipitating agents and the like. However, the polynucleotide of the present invention can also be delivered in liposome formulations and LIPOFECTIN™ formulations and the like can be prepared by methods well known to those skilled in the art. Such methods are described, for example, in U.S. Pat. Nos. 5,593,972, 5,589,466, and 5,580,859, which are herein incorporated by reference.

The polynucleotide vector constructs used in the gene therapy method are preferably constructs that will not integrate into the host genome nor will they contain sequences that allow for replication. Appropriate vectors include pWLNEO, pSV2CAT, pOG44, pXT1 and pSG available from STRATAGENE™; pSVK3, pBPV, pMSG and pSVL available from PHARMACIA™; and pEF1/V5, pcDNA3.1, and pRc/CMV2 available from Invitrogen. Other suitable vectors will be readily apparent to the skilled artisan.

Any strong promoter known to those skilled in the art can be used for driving the expression of the polynucleotide sequence. Suitable promoters include adenoviral promoters, such as the adenoviral major late promoter; or heterologous promoters, such as the cytomegalovirus (CMV) promoter; the respiratory syncytial virus (RSV) promoter; inducible promoters, such as the MMT promoter, the metallothionein promoter; heat shock promoters; the albumin promoter; the ApoAI promoter; human globin promoters; viral thymidine kinase promoters, such as the Herpes Simplex thymidine kinase promoter; retroviral LTRs; the b-actin promoter; and human growth hormone promoters. The promoter also may be the native promoter for the polynucleotide of the present invention.

Unlike other gene therapy techniques, one major advantage of introducing naked nucleic acid sequences into target cells is the transitory nature of the polynucleotide synthesis in the cells. Studies have shown that non-replicating DNA sequences can be introduced into cells to provide production of the desired polypeptide for periods of up to six months.

The polynucleotide construct can be delivered to the interstitial space of tissues within the an animal, including of muscle, skin, brain, lung, liver, spleen, bone marrow, thymus, heart, lymph, blood, bone, cartilage, pancreas, kidney, gall bladder, stomach, intestine, testis, ovary, uterus, rectum, nervous system, eye, gland, and connective tissue. Interstitial space of the tissues comprises the intercellular, fluid, mucopolysaccharide matrix among the reticular fibers of organ tissues, elastic fibers in the walls of vessels or chambers, collagen fibers of fibrous tissues, or that same matrix within connective tissue ensheathing muscle cells or in the lacunae of bone. It is similarly the space occupied by the plasma of the circulation and the lymph fluid of the lymphatic channels. Delivery to the interstitial space of muscle tissue is preferred for the reasons discussed below. They may be conveniently delivered by injection into the tissues comprising these cells. They are preferably delivered to and expressed in persistent, non-dividing cells which are differentiated, although delivery and expression may be achieved in non-differentiated or less completely differentiated cells, such as, for example, stem cells of blood or skin fibroblasts. In vivo muscle cells are particularly competent in their ability to take up and express polynucleotides.

For the naked nucleic acid sequence injection, an effective dosage amount of DNA or RNA will be in the range of from about 0.05 mg/kg body weight to about 50 mg/kg body weight. Preferably the dosage will be from about 0.005 mg/kg to about 20 mg/kg and more preferably from about 0.05 mg/kg to about 5 mg/kg. Of course, as the artisan of ordinary skill will appreciate, this dosage will vary according to the tissue site of injection. The appropriate and effective dosage of nucleic acid sequence can readily be determined by those of ordinary skill in the art and may depend on the condition being treated and the route of administration.

The preferred route of administration is by the parenteral route of injection into the interstitial space of tissues. However, other parenteral routes may also be used, such as, inhalation of an aerosol formulation particularly for delivery to lungs or bronchial tissues, throat or mucous membranes of the nose. In addition, naked DNA constructs can be delivered to arteries during angioplasty by the catheter used in the procedure.

The naked polynucleotides are delivered by any method known in the art, including, but not limited to, direct needle injection at the delivery site, intravenous injection, topical administration, catheter infusion, and so-called “gene guns”. These delivery methods are known in the art.

The constructs may also be delivered with delivery vehicles such as viral sequences, viral particles, liposome formulations, LIPOFECTIN™, precipitating agents, etc. Such methods of delivery are known in the art.

In certain embodiments, the polynucleotide constructs are complexed in a liposome preparation. Liposomal preparations for use in the instant invention include cationic (positively charged), anionic (negatively charged) and neutral preparations. However, cationic liposomes are particularly preferred because a tight charge complex can be formed between the cationic liposome and the polyanionic nucleic acid. Cationic liposomes have been shown to mediate intracellular delivery of plasmid DNA (Felgner et al., Proc. Natl. Acad. Sci. USA (1987) 84:7413-7416, which is herein incorporated by reference); mRNA (Malone et al., Proc. Natl. Acad. Sci. USA (1989) 86:6077-6081, which is herein incorporated by reference); and purified transcription factors (Debs et al., J. Biol. Chem. (1990) 265:10189-10192, which is herein incorporated by reference), in functional form.

Cationic liposomes are readily available. For example, N[1-2,3-dioleyloxy)propyl]-N,N,N-triethylammonium (DOTMA) liposomes are particularly useful and are available under the trademark LIPOFECTIN™, from GIBCO BRL, Grand Island, N.Y. (See, also, Felgner et al., Proc. Natl. Acad. Sci. USA (1987) 84:7413-7416, which is herein incorporated by reference). Other commercially available liposomes include transfectace (DDAB/DOPE) and DOTAP/DOPE (BOEHRINGER™).

Other cationic liposomes can be prepared from readily available materials using techniques well known in the art. See, e.g. PCT Publication No. WO 90/11092 (which is herein incorporated by reference) for a description of the synthesis of DOTAP (1,2-bis(oleoyloxy)-3-(trimethylammonio)propane) liposomes. Preparation of DOTMA liposomes is explained in the literature, see, e.g., P. Felgner et al., Proc. Natl. Acad. Sci. USA 84:7413-7417, which is herein incorporated by reference. Similar methods can be used to prepare liposomes from other cationic lipid materials.

Similarly, anionic and neutral liposomes are readily available, such as from Avanti Polar Lipids (Birmingham, Ala.), or can be easily prepared using readily available materials. Such materials include phosphatidyl, choline, cholesterol, phosphatidyl ethanolamine, dioleoylphosphatidyl choline (DOPC), dioleoylphosphatidyl glycerol (DOPG), dioleoylphoshatidyl ethanolamine (DOPE), among others. These materials can also be mixed with the DOTMA and DOTAP starting materials in appropriate ratios. Methods for making liposomes using these materials are well known in the art.

For example, commercially dioleoylphosphatidyl choline (DOPC), dioleoylphosphatidyl glycerol (DOPG), and dioleoylphosphatidyl ethanolamine (DOPE) can be used in various combinations to make conventional liposomes, with or without the addition of cholesterol. Thus, for example, DOPG/DOPC vesicles can be prepared by drying 50 mg each of DOPG and DOPC under a stream of nitrogen gas into a sonication vial. The sample is placed under a vacuum pump overnight and is hydrated the following day with deionized water. The sample is then sonicated for 2 hours in a capped vial, using a Heat Systems model 350 sonicator equipped with an inverted cup (bath type) probe at the maximum setting while the bath is circulated at 15EC. Alternatively, negatively charged vesicles can be prepared without sonication to produce multilamellar vesicles or by extrusion through nucleopore membranes to produce unilamellar vesicles of discrete size. Other methods are known and available to those of skill in the art.

The liposomes can comprise multilamellar vesicles (MLVs), small unilamellar vesicles (SUVs), or large unilamellar vesicles (LUVs), with SUVs being preferred. The various liposome-nucleic acid complexes are prepared using methods well known in the art. See, e.g., Straubinger et al., Methods of Immunology (1983), 101:512-527, which is herein incorporated by reference. For example, MLVs containing nucleic acid can be prepared by depositing a thin film of phospholipid on the walls of a glass tube and subsequently hydrating with a solution of the material to be encapsulated. SUVs are prepared by extended sonication of MLVs to produce a homogeneous population of unilamellar liposomes. The material to be entrapped is added to a suspension of preformed MLVs and then sonicated. When using liposomes containing cationic lipids, the dried lipid film is resuspended in an appropriate solution such as sterile water or an isotonic buffer solution such as 10 mM Tris/NaCl, sonicated, and then the preformed liposomes are mixed directly with the DNA. The liposome and DNA form a very stable complex due to binding of the positively charged liposomes to the cationic DNA. SUVs find use with small nucleic acid fragments. LUVs are prepared by a number of methods, well known in the art. Commonly used methods include Ca²⁺-EDTA chelation (Papahadjopoulos et al., Biochim. Biophys. Acta (1975) 394:483; Wilson et al., Cell 17:77 (1979)); ether injection (Deamer, D. and Bangham, A., Biochim. Biophys. Acta 443:629 (1976); Ostro et al., Biochem. Biophys. Res. Commun. 76:836 (1977); Fraley et al., Proc. Natl. Acad. Sci. USA 76:3348 (1979)); detergent dialysis (Enoch, H. and Strittmatter, P., Proc. Natl. Acad. Sci. USA 76:145 (1979)); and reverse-phase evaporation (REV) (Fraley et al., J. Biol. Chem. 255:10431 (1980); Szoka, F. and Papahadjopoulos, D., Proc. Natl. Acad. Sci. USA 75:145 (1978); Schaefer-Ridder et al., Science 215:166 (1982)), which are herein incorporated by reference.

Generally, the ratio of DNA to liposomes will be from about 10:1 to about 1:10. Preferably, the ration will be from about 5:1 to about 1:5. More preferably, the ration will be about 3:1 to about 1:3. Still more preferably, the ratio will be about 1:1.

U.S. Pat. No. 5,676,954 (which is herein incorporated by reference) reports on the injection of genetic material, complexed with cationic liposomes carriers, into mice. U.S. Pat. Nos. 4,897,355, 4,946,787, 5,049,386, 5,459,127, 5,589,466, 5,693,622, 5,580,859, 5,703,055, and international publication no. WO 94/9469 (which are herein incorporated by reference) provide cationic lipids for use in transfecting DNA into cells and mammals. U.S. Pat. Nos. 5,589,466, 5,693,622, 5,580,859, 5,703,055, and international publication no. WO 94/9469 provide methods for delivering DNA-cationic lipid complexes to mammals.

In certain embodiments, cells are engineered, ex vivo or in vivo, using a retroviral particle containing RNA which comprises a sequence encoding a polypeptide of the present invention. Retroviruses from which the retroviral plasmid vectors may be derived include, but are not limited to, Moloney Murine Leukemia Virus, spleen necrosis virus, Rous sarcoma Virus, Harvey Sarcoma Virus, avian leukosis virus, gibbon ape leukemia virus, human immunodeficiency virus, Myeloproliferative Sarcoma Virus, and mammary tumor virus.

The retroviral plasmid vector is employed to transduce packaging cell lines to form producer cell lines. Examples of packaging cells which may be transfected include, but are not limited to, the PE501, PA317, R-2, R-AM, PA12, T19-14×, VT-19-17-H2, RCRE, RCRIP, GP+E-86, GP+envAm12, and DAN cell lines as described in Miller, Human Gene Therapy 1:5-14 (1990), which is incorporated herein by reference in its entirety. The vector may transduce the packaging cells through any means known in the art. Such means include, but are not limited to, electroporation, the use of liposomes, and CaPO₄ precipitation. In one alternative, the retroviral plasmid vector may be encapsulated into a liposome, or coupled to a lipid, and then administered to a host.

The producer cell line generates infectious retroviral vector particles which include polynucleotide encoding a polypeptide of the present invention. Such retroviral vector particles then may be employed, to transduce eukaryotic cells, either in vitro or in vivo. The transduced eukaryotic cells will express a polypeptide of the present invention.

In certain other embodiments, cells are engineered, ex vivo or in vivo, with polynucleotide contained in an adenovirus vector. Adenovirus can be manipulated such that it encodes and expresses a polypeptide of the present invention, and at the same time is inactivated in terms of its ability to replicate in a normal lytic viral life cycle. Adenovirus expression is achieved without integration of the viral DNA into the host cell chromosome, thereby alleviating concerns about insertional mutagenesis. Furthermore, adenoviruses have been used as live enteric vaccines for many years with an excellent safety profile (Schwartz et al. Am. Rev. Respir. Dis.109:233-238 (1974)). Finally, adenovirus mediated gene transfer has been demonstrated in a number of instances including transfer of alpha-1-antitrypsin and CFTR to the lungs of cotton rats (Rosenfeld, M. A. et al. (1991) Science 252:431-434; Rosenfeld et al., (1992) Cell 68:143-155). Furthermore, extensive studies to attempt to establish adenovirus as a causative agent in human cancer were uniformly negative (Green, M. et al. (1979) Proc. Natl. Acad. Sci. USA 76:6606).

Suitable adenoviral vectors useful in the present invention are described, for example, in Kozarsky and Wilson, Curr. Opin. Genet. Devel. 3:499-503 (1993); Rosenfeld et al., Cell 68:143-155 (1992); Engelhardt et al., Human Genet. Ther. 4:759-769 (1993); Yang et al., Nature Genet. 7:362-369 (1994); Wilson et al., Nature 365:691-692 (1993); and U.S. Pat. No. 5,652,224, which are herein incorporated by reference. For example, the adenovirus vector Ad2 is useful and can be grown in human 293 cells. These cells contain the E1 region of adenovirus and constitutively express E1a and E1b, which complement the defective adenoviruses by providing the products of the genes deleted from the vector. In addition to Ad2, other varieties of adenovirus (e.g., Ad3, Ad5, and Ad7) are also useful in the present invention.

Preferably, the adenoviruses used in the present invention are replication deficient. Replication deficient adenoviruses require the aid of a helper virus and/or packaging cell line to form infectious particles. The resulting virus is capable of infecting cells and can express a polynucleotide of interest which is operably linked to a promoter, but cannot replicate in most cells. Replication deficient adenoviruses may be deleted in one or more of all or a portion of the following genes: E1a, E1b, E3, E4, E2a, or L1 through L5.

In certain other embodiments, the cells are engineered, ex vivo or in vivo, using an adeno-associated virus (AAV). AAVs are naturally occurring defective viruses that require helper viruses to produce infectious particles (Muzyczka, N., Curr. Topics in Microbiol. Immunol. 158:97 (1992)). It is also one of the few viruses that may integrate its DNA into non-dividing cells. Vectors containing as little as 300 base pairs of AAV can be packaged and can integrate, but space for exogenous DNA is limited to about 4.5 kb. Methods for producing and using such AAVs are known in the art. See, for example, U.S. Pat. Nos. 5,139,941, 5,173,414, 5,354,678, 5,436,146, 5,474,935, 5,478,745, and 5,589,377.

For example, an appropriate AAV vector for use in the present invention will include all the sequences necessary for DNA replication, encapsidation, and host-cell integration. The polynucleotide construct is inserted into the AAV vector using standard cloning methods, such as those found in Sambrook et al., Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Press (1989). The recombinant AAV vector is then transfected into packaging cells which are infected with a helper virus, using any standard technique, including lipofection, electroporation, calcium phosphate precipitation, etc. Appropriate helper viruses include adenoviruses, cytomegaloviruses, vaccinia viruses, or herpes viruses. Once the packaging cells are transfected and infected, they will produce infectious AAV viral particles which contain the polynucleotide construct. These viral particles are then used to transduce eukaryotic cells, either ex vivo or in vivo. The transduced cells will contain the polynucleotide construct integrated into its genome, and will express a polypeptide of the invention.

Another method of gene therapy involves operably associating heterologous control regions and endogenous polynucleotide sequences (e.g. encoding a polypeptide of the present invention) via homologous recombination (see, e.g., U.S. Pat. No. 5,641,670, issued Jun. 24, 1997; International Publication No. WO 96/29411, published Sep. 26, 1996; International Publication No. WO 94/12650, published Aug. 4, 1994; Koller et al., Proc. Natl. Acad. Sci. USA 86:8932-8935 (1989); and Zijlstra et al., Nature 342:435-438 (1989), which are herein encorporated by reference. This method involves the activation of a gene which is present in the target cells, but which is not normally expressed in the cells, or is expressed at a lower level than desired.

Polynucleotide constructs are made, using standard techniques known in the art, which contain the promoter with targeting sequences flanking the promoter. Suitable promoters are described herein. The targeting sequence is sufficiently complementary to an endogenous sequence to permit homologous recombination of the promoter-targeting sequence with the endogenous sequence. The targeting sequence will be sufficiently near the 5′ end of the desired endogenous polynucleotide sequence so the promoter will be operably linked to the endogenous sequence upon homologous recombination.

The promoter and the targeting sequences can be amplified using PCR. Preferably, the amplified promoter contains distinct restriction enzyme sites on the 5′ and 3′ ends. Preferably, the 3′ end of the first targeting sequence contains the same restriction enzyme site as the 5′ end of the amplified promoter and the 5′ end of the second targeting sequence contains the same restriction site as the 3′ end of the amplified promoter. The amplified promoter and targeting sequences are digested and ligated together.

The promoter-targeting sequence construct is delivered to the cells, either as naked polynucleotide, or in conjunction with transfection-facilitating agents, such as liposomes, viral sequences, viral particles, whole viruses, lipofection, precipitating agents, etc., described in more detail above. The P promoter-targeting sequence can be delivered by any method, included direct needle injection, intravenous injection, topical administration, catheter infusion, particle accelerators, etc. The methods are described in more detail below.

The promoter-targeting sequence construct is taken up by cells. Homologous recombination between the construct and the endogenous sequence takes place, such that an endogenous sequence is placed under the control of the promoter. The promoter then drives the expression of the endogenous sequence.

The polynucleotide encoding a polypeptide of the present invention may contain a secretory signal sequence that facilitates secretion of the protein. Typically, the signal sequence is positioned in the coding region of the polynucleotide to be expressed towards or at the 5′ end of the coding region. The signal sequence may be homologous or heterologous to the polynucleotide of interest and may be homologous or heterologous to the cells to be transfected. Additionally, the signal sequence may be chemically synthesized using methods known in the art.

Any mode of administration of any of the above-described polynucleotides constructs can be used so long as the mode results in the expression of one or more molecules in an amount sufficient to provide a therapeutic effect. This includes direct needle injection, systemic injection, catheter infusion, biolistic injectors, particle accelerators (i.e., “gene guns”), gelfoam sponge depots, other commercially available depot materials, osmotic pumps (e.g., Alza minipumps), oral or suppositorial solid (tablet or pill) pharmaceutical formulations, and decanting or topical applications during surgery. For example, direct injection of naked calcium phosphate-precipitated plasmid into rat liver and rat spleen or a protein-coated plasmid into the portal vein has resulted in gene expression of the foreign gene in the rat livers (Kaneda et al., Science 243:375 (1989)).

A preferred method of local administration is by direct injection. Preferably, a recombinant molecule of the present invention complexed with a delivery vehicle is administered by direct injection into or locally within the area of arteries. Administration of a composition locally within the area of arteries refers to injecting the composition centimeters and preferably, millimeters within arteries.

Another method of local administration is to contact a polynucleotide construct of the present invention in or around a surgical wound. For example, a patient can undergo surgery and the polynucleotide construct can be coated on the surface of tissue inside the wound or the construct can be injected into areas of tissue inside the wound.

Therapeutic compositions useful in systemic administration, include recombinant molecules of the present invention complexed to a targeted delivery vehicle of the present invention. Suitable delivery vehicles for use with systemic administration comprise liposomes comprising ligands for targeting the vehicle to a particular site. In specific embodiments, suitable delivery vehicles for use with systemic administration comprise liposomes comprising polypeptides of the invention for targeting the vehicle to a particular site.

Preferred methods of systemic administration, include intravenous injection, aerosol, oral and percutaneous (topical) delivery. Intravenous injections can be performed using methods standard in the art. Aerosol delivery can also be performed using methods standard in the art (see, for example, Stribling et al., Proc. Natl. Acad. Sci. USA 189:11277-11281, 1992, which is incorporated herein by reference). Oral delivery can be performed by complexing a polynucleotide construct of the present invention to a carrier capable of withstanding degradation by digestive enzymes in the gut of an animal. Examples of such carriers, include plastic capsules or tablets, such as those known in the art. Topical delivery can be performed by mixing a polynucleotide construct of the present invention with a lipophilic reagent (e.g., DMSO) that is capable of passing into the skin.

Determining an effective amount of substance to be delivered can depend upon a number of factors including, for example, the chemical structure and biological activity of the substance, the age and weight of the animal, the precise condition requiring treatment and its severity, and the route of administration. The frequency of treatments depends upon a number of factors, such as the amount of polynucleotide constructs administered per dose, as well as the health and history of the subject. The precise amount, number of doses, and timing of doses will be determined by the attending physician or veterinarian.

Therapeutic compositions of the present invention can be administered to any animal, preferably to mammals and birds. Preferred mammals include humans, dogs, cats, mice, rats, rabbits sheep, cattle, horses and pigs, with humans being particularly preferred.

Biological Activities

Polynucleotides or polypeptides, or agonists or antagonists of the present invention, can be used in assays to test for one or more biological activities. If these polynucleotides or polypeptides, or agonists or antagonists of the present invention, do exhibit activity in a particular assay, it is likely that these molecules may be involved in the diseases associated with the biological activity. Thus, the polynucleotides and polypeptides, and agonists or antagonists could be used to treat the associated disease.

Members of the secreted family of proteins are believed to be involved in biological activities associated with, for example, cellular signaling. Accordingly, compositions of the invention (including polynucleotides, polypeptides and antibodies of the invention, and fragments and variants thereof) may be used in diagnosis, prognosis, prevention and/or treatment of diseases and/or disorders associated with aberrant activity of secreted polypeptides.

In preferred embodiments, compositions of the invention (including polynucleotides, polypeptides and antibodies of the invention, and fragments and variants thereof) may be used in the diagnosis, prognosis, prevention, treatment, and/or amelioration of cancer and other hyperproliferative diseases and/or disorders (e.g., as described in the “Hyperproliferative Disorders”). In certain embodiments, a polypeptide of the invention, or polynucleotides, antibodies, agonists, or antagonists corresponding to that polypeptide, may be used to diagnose and/or prognosticate diseases and/or disorders associated with the tissue(s) in which the polypeptide of the invention is expressed including one, two, three, four, five, or more tissues disclosed in Table 1B.2, column 5 (Tissue Distribution Library Code).

Thus, polynucleotides, translation products and antibodies of the invention are useful in the diagnosis, detection, prevention, prognistication, and/or treatment of diseases and/or disorders associated with activities that include, but are not limited to, prohormone activation, neurotransmitter activity, cellular signaling, cellular proliferation, cellular differentiation, and cell migration.

More generally, polynucleotides, translation products and antibodies corresponding to this gene may be useful for the diagnosis, prognosis, prevention, treatment and/or amelioration of diseases and/or disorders associated with the following system or systems.

Immune Activity

Polynucleotides, polypeptides, antibodies, and/or agonists or antagonists of the present invention may be useful in preventing, diagnosing, prognosticating, treating, and/or ameliorating diseases, disorders, and/or conditions of the immune system, by, for example, activating or inhibiting the proliferation, differentiation, or mobilization (chemotaxis) of immune cells. Immune cells develop through a process called hematopoiesis, producing myeloid (platelets, red blood cells, neutrophils, and macrophages) and lymphoid (B and T lymphocytes) cells from pluripotent stem cells. The etiology of these immune diseases, disorders, and/or conditions may be genetic, somatic, such as cancer and some autoimmune diseases, acquired (e.g., by chemotherapy or toxins), or infectious. Moreover, polynucleotides, polypeptides, antibodies, and/or agonists or antagonists of the present invention can be used as a marker or detector of a particular immune system disease or disorder.

In another embodiment, a polypeptide of the invention, or polynucleotides, antibodies, agonists, or antagonists corresponding to that polypeptide, may be used to treat diseases and disorders of the immune system and/or to inhibit or enhance an immune response generated by cells associated with the tissue(s) in which the polypeptide of the invention is expressed, including one, two, three, four, five, or more tissues disclosed in Table 1B.2, column 5 (Tissue Distribution Library Code).

Polynucleotides, polypeptides, antibodies, and/or agonists or antagonists of the present invention may be useful in preventing, diagnosing, prognosticating, treating and/or ameliorating immunodeficiencies, including both congenital and acquired immunodeficiencies. Examples of B cell immunodeficiencies in which immunoglobulin levels B cell function and/or B cell numbers are decreased include: X-linked agammaglobulinemia (Bruton's disease), X-linked infantile agammaglobulinemia, X-linked immunodeficiency with hyper IgM, non X-linked immunodeficiency with hyper IgM, X-linked lymphoproliferative syndrome (XLP), agammaglobulinemia including congenital and acquired agammaglobulinemia, adult onset agammaglobulinemia, late-onset agammaglobulinemia, dysgammaglobulinemia, hypogammaglobulinemia, unspecified hypogammaglobulinemia, recessive agammaglobulinemia (Swiss type), Selective IgM deficiency, selective IgA deficiency, selective IgG subclass deficiencies, IgG subclass deficiency (with or without IgA deficiency), Ig deficiency with increased IgM, IgG and IgA deficiency with increased IgM, antibody deficiency with normal or elevated Igs, Ig heavy chain deletions, kappa chain deficiency, B cell lymphoproliferative disorder (BLPD), common variable immunodeficiency (CVID), common variable immunodeficiency (CVI) (acquired), and transient hypogammaglobulinemia of infancy.

In specific embodiments, ataxia-telangiectasia or conditions associated with ataxia-telangiectasia are detected, prevented, diagnosed, prognosticated, treated, and/or ameliorated using the polypeptides or polynucleotides of the invention, and/or agonists or antagonists thereof.

Examples of congenital immunodeficiencies in which T cell and/or B cell function and/or number is decreased include, but are not limited to: DiGeorge anomaly, severe combined immunodeficiencies (SCID) (including, but not limited to, X-linked SCID, autosomal recessive SCID, adenosine deaminase deficiency, purine nucleoside phosphorylase (PNP) deficiency, Class II MHC deficiency (Bare lymphocyte syndrome), Wiskott-Aldrich syndrome, and ataxia telangiectasia), thymic hypoplasia, third and fourth pharyngeal pouch syndrome, 22q11.2 deletion, chronic mucocutaneous candidiasis, natural killer cell deficiency (NK), idiopathic CD4+ T-lymphocytopenia, immunodeficiency with predominant T cell defect (unspecified), and unspecified immunodeficiency of cell mediated immunity.

In specific embodiments, DiGeorge anomaly or conditions associated with DiGeorge anomaly are prevented, detected, diagnosed, prognosticated, treated and/or ameliorated using polypeptides or polynucleotides of the invention, or antagonists or agonists thereof.

Other immunodeficiencies that may be prevented, detected, diagnosed, prognosticated, treated and/or ameliorated using polypeptides or polynucleotides of the invention, and/or agonists or antagonists thereof, include, but are not limited to, chronic granulomatous disease, Chediak-Higashi syndrome, myeloperoxidase deficiency, leukocyte glucose-6-phosphate dehydrogenase deficiency, X-linked lymphoproliferative syndrome (XLP), leukocyte adhesion deficiency, complement component deficiencies (including C1, C2, C3, C4, C5, C6, C7, C8 and/or C9 deficiencies), reticular dysgenesis, thymic alymphoplasia-aplasia, immunodeficiency with thymoma, severe congenital leukopenia, dysplasia with immunodeficiency, neonatal neutropenia, short limbed dwarfism, and Nezelof syndrome-combined immunodeficiency with Igs.

In a preferred embodiment, the immunodeficiencies and/or conditions associated with the immunodeficiencies recited above are prevented, detected, diagnosed, prognosticated, treated and/or ameliorated using polynucleotides, polypeptides, antibodies, and/or agonists or antagonists of the present invention.

In a preferred embodiment polynucleotides, polypeptides, antibodies, and/or agonists or antagonists of the present invention could be used as an agent to boost immunoresponsiveness among immunodeficient individuals. In specific embodiments, polynucleotides, polypeptides, antibodies, and/or agonists or antagonists of the present invention could be used as an agent to boost immunoresponsiveness among B cell and/or T cell immunodeficient individuals.

The polynucleotides, polypeptides, antibodies, and/or agonists or antagonists of the present invention may be useful in preventing, detecting, diagnosing, prognosticating, treating and/or ameliorating autoimmune disorders. Many autoimmune disorders result from inappropriate recognition of self as foreign material by immune cells. This inappropriate recognition results in an immune response leading to the destruction of the host tissue. Therefore, the administration of polynucleotides and polypeptides of the invention that can inhibit an immune response, particularly the proliferation, differentiation, or chemotaxis of T-cells, may be an effective therapy in preventing autoimmune disorders.

Autoimmune diseases or disorders that may be prevented, detected, diagnosed, prognosticated, treated, and/or ameliorated by polynucleotides, polypeptides, antibodies, and/or agonists or antagonists of the present invention include, but are not limited to, one or more of the following: systemic lupus erythematosus, rheumatoid arthritis, ankylosing spondylitis, multiple sclerosis, autoimmune thyroiditis, Hashimoto's thyroiditis, autoimmune hemolytic anemia, hemolytic anemia, thrombocytopenia, autoimmune thrombocytopenia purpura, autoimmune neonatal thrombocytopenia, idiopathic thrombocytopenia purpura, purpura (e.g., Henloch-Scoenlein purpura), autoimmunocytopenia, Goodpasture's syndrome, Pemphigus vulgaris, myasthenia gravis, Grave's disease (hyperthyroidism), and insulin-resistant diabetes mellitus.

Additional disorders that are likely to have an autoimmune component that may be prevented, detected, diagnosed, prognosticated, treated and/or ameliorated with the compositions of the invention include, but are not limited to, type II collagen-induced arthritis, antiphospholipid syndrome, dermatitis, allergic encephalomyelitis, myocarditis, relapsing polychondritis, rheumatic heart disease, neuritis, uveitis ophthalmia, polyendocrinopathies, Reiter's Disease, Stiff-Man Syndrome, autoimmune pulmonary inflammation, autism, Guillain-Barre Syndrome, insulin dependent diabetes mellitus, and autoimmune inflammatory eye disorders.

Additional disorders that are likely to have an autoimmune component that may be prevented, detected, diagnosed, prognosticated, treated and/or ameliorated with the compositions of the invention include, but are not limited to, scleroderma with anti-collagen antibodies (often characterized, e.g., by nucleolar and other nuclear antibodies), mixed connective tissue disease (often characterized, e.g., by antibodies to extractable nuclear antigens (e.g., ribonucleoprotein)), polymyositis (often characterized, e.g., by nonhistone ANA), pernicious anemia (often characterized, e.g., by antiparietal cell, microsomes, and intrinsic factor antibodies), idiopathic Addison's disease (often characterized, e.g., by humoral and cell-mediated adrenal cytotoxicity, infertility (often characterized, e.g., by antispermatozoal antibodies), glomerulonephritis (often characterized, e.g., by glomerular basement membrane antibodies or immune complexes), bullous pemphigoid (often characterized, e.g., by IgG and complement in basement membrane), Sjogren's syndrome (often characterized, e.g., by multiple tissue antibodies, and/or a specific nonhistone ANA (SS-B)), diabetes mellitus (often characterized, e.g., by cell-mediated and humoral islet cell antibodies), and adrenergic drug resistance (including adrenergic drug resistance with asthma or cystic fibrosis) (often characterized, e.g., by beta-adrenergic receptor antibodies).

Additional disorders that may have an autoimmune component that may be prevented, detected, diagnosed, prognosticated, treated and/or ameliorated with the compositions of the invention include, but are not limited to, chronic active hepatitis (often characterized, e.g., by smooth muscle antibodies), primary biliary cirrhosis (often characterized, e.g., by mitochondria antibodies), other endocrine gland failure (often characterized, e.g., by specific tissue antibodies in some cases), vitiligo (often characterized, e.g., by melanocyte antibodies), vasculitis (often characterized, e.g., by Ig and complement in vessel walls and/or low serum complement), post-Ml (often characterized, e.g., by myocardial antibodies), cardiotomy syndrome (often characterized, e.g., by myocardial antibodies), urticaria (often characterized, e.g., by IgG and IgM antibodies to IgE), atopic dermatitis (often characterized, e.g., by IgG and IgM antibodies to IgE), asthma (often characterized, e.g., by IgG and IgM antibodies to IgE), and many other inflammatory, granulomatous, degenerative, and atrophic disorders.

In a preferred embodiment, the autoimmune diseases and disorders and/or conditions associated with the diseases and disorders recited above are prevented, detected, diagnosed, prognosticated, treated and/or ameliorated using for example, antagonists or agonists, polypeptides or polynucleotides, or antibodies of the present invention. In a specific preferred embodiment, rheumatoid arthritis is prevented, detected, diagnosed, prognosticated, treated and/or ameliorated using polynucleotides, polypeptides, antibodies, and/or agonists or antagonists of the present invention.

In another specific preferred embodiment, systemic lupus erythematosus is prevented, detected, diagnosed, prognosticated, treated and/or ameliorated using polynucleotides, polypeptides, antibodies, and/or agonists or antagonists of the present invention. In another specific preferred embodiment, idiopathic thrombocytopenia purpura is prevented, detected, diagnosed, prognosticated, treated and/or ameliorated using polynucleotides, polypeptides, antibodies, and/or agonists or antagonists of the present invention.

In another specific preferred embodiment IgA nephropathy is prevented, detected, diagnosed, prognosticated, treated and/or ameliorated using polynucleotides, polypeptides, antibodies, and/or agonists or antagonists of the present invention.

In a preferred embodiment, the autoimmune diseases and disorders and/or conditions associated with the diseases and disorders recited above are prevented, detected, diagnosed, prognosticated, treated and/or ameliorated using polynucleotides, polypeptides, antibodies, and/or agonists or antagonists of the present invention

In preferred embodiments, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention are used as a immunosuppressive agent(s).

Polynucleotides, polypeptides, antibodies, and/or agonists or antagonists of the present invention may be useful in detecting, preventing, diagnosing, prognosticating, treating, and/or ameliorating diseases, disorders, and/or conditions of hematopoietic cells. Polynucleotides, polypeptides, antibodies, and/or agonists or antagonists of the present invention could be used to increase differentiation and proliferation of hematopoietic cells, including the pluripotent stem cells, in an effort to treat or prevent those diseases, disorders, and/or conditions associated with a decrease in certain (or many) types hematopoietic cells, including but not limited to, leukopenia, neutropenia, anemia, and thrombocytopenia. Alternatively, Polynucleotides, polypeptides, antibodies, and/or agonists or antagonists of the present invention could be used to increase differentiation and proliferation of hematopoietic cells, including the pluripotent stem cells, in an effort to treat or prevent those diseases, disorders, and/or conditions associated with an increase in certain (or many) types of hematopoietic cells, including but not limited to, histiocytosis.

Allergic reactions and conditions, such as asthma (particularly allergic asthma) or other respiratory problems, may also be detected, prevented, diagnosed, prognosticated, treated, and/or ameliorated using polypeptides, antibodies, or polynucleotides of the invention, and/or agonists or antagonists thereof. Moreover, these molecules can be used to treat, prevent, prognose, and/or diagnose anaphylaxis, hypersensitivity to an antigenic molecule, or blood group incompatibility.

Additionally, polypeptides or polynucleotides of the invention, and/or agonists or antagonists thereof, may be used to detect, prevent, diagnose, prognosticate, treat, and/or ameliorate IgE-mediated allergic reactions. Such allergic reactions include, but are not limited to, asthma, rhinitis, and eczema. In specific embodiments, polynucleotides, polypeptides, antibodies, and/or agonists or antagonists of the present invention may be used to modulate IgE concentrations in vitro or in vivo.

Moreover, polynucleotides, polypeptides, antibodies, and/or agonists or antagonists of the present invention have uses in the detection, prevention, diagnosis, prognostication, treatment, and/or amelioration of inflammatory conditions. For example, since polypeptides, antibodies, or polynucleotides of the invention, and/or agonists or antagonists of the invention may inhibit the activation, proliferation and/or differentiation of cells involved in an inflammatory response, these molecules can be used to prevent and/or treat chronic and acute inflammatory conditions. Such inflammatory conditions include, but are not limited to, for example, inflammation associated with infection (e.g., septic shock, sepsis, or systemic inflammatory response syndrome), ischemia-reperfusion injury, endotoxin lethality, complement-mediated hyperacute rejection, nephritis, cytokine or chemokine induced lung injury, inflammatory bowel disease, Crohn's disease, over production of cytokines (e.g., TNF or IL-1.), respiratory disorders (e.g., asthma and allergy); gastrointestinal disorders (e.g., inflammatory bowel disease); cancers (e.g., gastric, ovarian, lung, bladder, liver, and breast); CNS disorders (e.g., multiple sclerosis; ischemic brain injury and/or stroke, traumatic brain injury, neurodegenerative disorders (e.g., Parkinson's disease and Alzheimer's disease); AIDS-related dementia; and prion disease); cardiovascular disorders (e.g., atherosclerosis, myocarditis, cardiovascular disease, and cardiopulmonary bypass complications); as well as many additional diseases, conditions, and disorders that are characterized by inflammation (e.g., hepatitis, rheumatoid arthritis, gout, trauma, pancreatitis, sarcoidosis, dermatitis, renal ischemia-reperfusion injury, Grave's disease, systemic lupus erythematosus, diabetes mellitus, and allogenic transplant rejection).

Because inflammation is a fundamental defense mechanism, inflammatory disorders can effect virtually any tissue of the body. Accordingly, polynucleotides, polypeptides, and antibodies of the invention, as well as agonists or antagonists thereof, have uses in the treatment of tissue-specific inflammatory disorders, including, but not limited to, adrenalitis, alveolitis, angiocholecystitis, appendicitis, balanitis, blepharitis, bronchitis, bursitis, carditis, cellulitis, cervicitis, cholecystitis, chorditis, cochlitis, colitis, conjunctivitis, cystitis, dermatitis, diverticulitis, encephalitis, endocarditis, esophagitis, eustachitis, fibrositis, folliculitis, gastritis, gastroenteritis, gingivitis, glossitis, hepatosplenitis, keratitis, labyrinthitis, laryngitis, lymphangitis, mastitis, media otitis, meningitis, metritis, mucitis, myocarditis, myosititis, myringitis, nephritis, neuritis, orchitis, osteochondritis, otitis, pericarditis, peritendonitis, peritonitis, pharyngitis, phlebitis, poliomyelitis, prostatitis, pulpitis, retinitis, rhinitis, salpingitis, scleritis, sclerochoroiditis, scrotitis, sinusitis, spondylitis, steatitis, stomatitis, synovitis, syringitis, tendonitis, tonsillitis, urethritis, and vaginitis.

In specific embodiments, polypeptides, antibodies, or polynucleotides of the invention, and/or agonists or antagonists thereof, are useful to detect, prevent, diagnose, prognosticate, treat, and/or ameliorate organ transplant rejections and graft-versus-host disease. Organ rejection occurs by host immune cell destruction of the transplanted tissue through an immune response. Similarly, an immune response is also involved in GVHD, but, in this case, the foreign transplanted immune cells destroy the host tissues. Polypeptides, antibodies, or polynucleotides of the invention, and/or agonists or antagonists thereof, that inhibit an immune response, particularly the activation, proliferation, differentiation, or chemotaxis of T-cells, may be an effective therapy in preventing organ rejection or GVHD. In specific embodiments, polypeptides, antibodies, or polynucleotides of the invention, and/or agonists or antagonists thereof, that inhibit an immune response, particularly the activation, proliferation, differentiation, or chemotaxis of T-cells, may be an effective therapy in preventing experimental allergic and hyperacute xenograft rejection.

In other embodiments, polypeptides, antibodies, or polynucleotides of the invention, and/or agonists or antagonists thereof, are useful to detect, prevent, diagnose, prognosticate, treat, and/or ameliorate immune complex diseases, including, but not limited to, serum sickness, post streptococcal glomerulonephritis, polyarteritis nodosa, and immune complex-induced vasculitis.

Polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the invention can be used to treat, detect, and/or prevent infectious agents. For example, by increasing the immune response, particularly increasing the proliferation activation and/or differentiation of B and/or T cells, infectious diseases may be treated, detected, and/or prevented. The immune response may be increased by either enhancing an existing immune response, or by initiating a new immune response. Alternatively, polynucleotides, polypeptides, antibodies, and/or agonists or antagonists of the present invention may also directly inhibit the infectious agent (refer to section of application listing infectious agents, etc), without necessarily eliciting an immune response.

In another embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention are used as a vaccine adjuvant that enhances immune responsiveness to an antigen. In a specific embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention are used as an adjuvant to enhance tumor-specific immune responses.

In another specific embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention are used as an adjuvant to enhance anti-viral immune responses. Anti-viral immune responses that may be enhanced using the compositions of the invention as an adjuvant, include virus and virus associated diseases or symptoms described herein or otherwise known in the art. In specific embodiments, the compositions of the invention are used as an adjuvant to enhance an immune response to a virus, disease, or symptom selected from the group consisting of: AIDS, meningitis, Dengue, EBV, and hepatitis (e.g., hepatitis B). In another specific embodiment, the compositions of the invention are used as an adjuvant to enhance an immune response to a virus, disease, or symptom selected from the group consisting of: HIV/AIDS, respiratory syncytial virus, Dengue, rotavirus, Japanese B encephalitis, influenza A and B, parainfluenza, measles, cytomegalovirus, rabies, Junin, Chikungunya, Rift Valley Fever, herpes simplex, and yellow fever.

In another specific embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention are used as an adjuvant to enhance anti-bacterial or anti-fungal immune responses. Anti-bacterial or anti-fungal immune responses that may be enhanced using the compositions of the invention as an adjuvant, include bacteria or fungus and bacteria or fungus associated diseases or symptoms described herein or otherwise known in the art. In specific embodiments, the compositions of the invention are used as an adjuvant to enhance an immune response to a bacteria or fungus, disease, or symptom selected from the group consisting of: tetanus, Diphtheria, botulism, and meningitis type B.

In another specific embodiment, the compositions of the invention are used as an adjuvant to enhance an immune response to a bacteria or fungus, disease, or symptom selected from the group consisting of: Vibrio cholerae, Mycobacterium leprae, Salmonella typhi, Salmonella paratyphi, Meisseria meningitidis, Streptococcus pneumoniae, Group B streptococcus, Shigella spp., Enterotoxigenic Escherichia coli, Enterohemorrhagic E. coli, and Borrelia burgdorferi.

In another specific embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention are used as an adjuvant to enhance anti-parasitic immune responses. Anti-parasitic immune responses that may be enhanced using the compositions of the invention as an adjuvant, include parasite and parasite associated diseases or symptoms described herein or otherwise known in the art. In specific embodiments, the compositions of the invention are used as an adjuvant to enhance an immune response to a parasite. In another specific embodiment, the compositions of the invention are used as an adjuvant to enhance an immune response to Plasmodium (malaria) or Leishmania.

In another specific embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention may also be employed to treat infectious diseases including silicosis, sarcoidosis, and idiopathic pulmonary fibrosis; for example, by preventing the recruitment and activation of mononuclear phagocytes.

In another specific embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention are used as an antigen for the generation of antibodies to inhibit or enhance immune mediated responses against polypeptides of the invention.

In one embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention are administered to an animal (e.g., mouse, rat, rabbit, hamster, guinea pig, pigs, micro-pig, chicken, camel, goat, horse, cow, sheep, dog, cat, non-human primate, and human, most preferably human) to boost the immune system to produce increased quantities of one or more antibodies (e.g., IgG, IgA, IgM, and IgE), to induce higher affinity antibody production and immunoglobulin class switching (e.g., IgG, IgA, IgM, and IgE), and/or to increase an immune response.

In another specific embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention are used as a stimulator of B cell responsiveness to pathogens.

In another specific embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention are used as an activator of T cells.

In another specific embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention are used as an agent that elevates the immune status of an individual prior to their receipt of immunosuppressive therapies.

In another specific embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention are used as an agent to induce higher affinity antibodies.

In another specific embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention are used as an agent to increase serum immunoglobulin concentrations.

In another specific embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention are used as an agent to accelerate recovery of immunocompromised individuals.

In another specific embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention are used as an agent to boost immunoresponsiveness among aged populations and/or neonates.

In another specific embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention are used as an immune system enhancer prior to, during, or after bone marrow transplant and/or other transplants (e.g., allogeneic or xenogeneic organ transplantation). With respect to transplantation, compositions of the invention may be administered prior to, concomitant with, and/or after transplantation. In a specific embodiment, compositions of the invention are administered after transplantation, prior to the beginning of recovery of T-cell populations. In another specific embodiment, compositions of the invention are first administered after transplantation after the beginning of recovery of T cell populations, but prior to full recovery of B cell populations.

In another specific embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention are used as an agent to boost immunoresponsiveness among individuals having an acquired loss of B cell function. Conditions resulting in an acquired loss of B cell function that may be ameliorated or treated by administering the polypeptides, antibodies, polynucleotides and/or agonists or antagonists thereof, include, but are not limited to, HIV Infection, AIDS, bone marrow transplant, and B cell chronic lymphocytic leukemia (CLL).

In another specific embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention are used as an agent to boost immunoresponsiveness among individuals having a temporary immune deficiency. Conditions resulting in a temporary immune deficiency that may be ameliorated or treated by administering the polypeptides, antibodies, polynucleotides and/or agonists or antagonists thereof, include, but are not limited to, recovery from viral infections (e.g., influenza), conditions associated with malnutrition, recovery from infectious mononucleosis, or conditions associated with stress, recovery from measles, recovery from blood transfusion, and recovery from surgery.

In another specific embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention are used as a regulator of antigen presentation by monocytes, dendritic cells, and/or B-cells. In one embodiment, polynucleotides, polypeptides, antibodies, and/or agonists or antagonists of the present invention enhance antigen presentation or antagonizes antigen presentation in vitro or in vivo. Moreover, in related embodiments, said enhancement or antagonism of antigen presentation may be useful as an anti-tumor treatment or to modulate the immune system.

In another specific embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention are used as an agent to direct an individual's immune system towards development of a humoral response (i.e. TH2) as opposed to a TH1 cellular response.

In another specific embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention are used as a means to induce tumor proliferation and thus make it more susceptible to anti-neoplastic agents. For example, multiple myeloma is a slowly dividing disease and is thus refractory to virtually all anti-neoplastic regimens. If these cells were forced to proliferate more rapidly their susceptibility profile would likely change.

In another specific embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention are used as a stimulator of B cell production in pathologies such as AIDS, chronic lymphocyte disorder and/or Common Variable Immunodeficiency.

In another specific embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention are used as a therapy for generation and/or regeneration of lymphoid tissues following surgery, trauma or genetic defect. In another specific embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention are used in the pretreatment of bone marrow samples prior to transplant.

In another specific embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention are used as a gene-based therapy for genetically inherited disorders resulting in immuno-incompetence/immunodeficiency such as observed among SCID patients.

In another specific embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention are used as a means of activating monocytes/macrophages to defend against parasitic diseases that effect monocytes such as Leishmania.

In another specific embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention are used as a means of regulating secreted cytokines that are elicited by polypeptides of the invention.

In another embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention are used in one or more of the applications described herein, as they may apply to veterinary medicine.

In another specific embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention are used as a means of blocking various aspects of immune responses to foreign agents or self. Examples of diseases or conditions in which blocking of certain aspects of immune responses may be desired include autoimmune disorders such as lupus, and arthritis, as well as immunoresponsiveness to skin allergies, inflammation, bowel disease, injury and diseases/disorders associated with pathogens.

In another specific embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention are used as a therapy for preventing the B cell proliferation and Ig secretion associated with autoimmune diseases such as idiopathic thrombocytopenic purpura, systemic lupus erythematosus and multiple sclerosis.

In another specific embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention are used as a inhibitor of B and/or T cell migration in endothelial cells. This activity disrupts tissue architecture or cognate responses and is useful, for example in disrupting immune responses, and blocking sepsis.

In another specific embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention are used as a therapy for chronic hypergammaglobulinemia evident in such diseases as monoclonal gammopathy of undetermined significance (MGUS), Waldenstrom's disease, related idiopathic monoclonal gammopathies, and plasmacytomas.

In another specific embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention may be employed for instance to inhibit polypeptide chemotaxis and activation of macrophages and their precursors, and of neutrophils, basophils, B lymphocytes and some T-cell subsets, e.g., activated and CD8 cytotoxic T cells and natural killer cells, in certain autoimmune and chronic inflammatory and infective diseases. Examples of autoimmune diseases are described herein and include multiple sclerosis, and insulin-dependent diabetes.

The polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention may also be employed to treat idiopathic hyper-eosinophilic syndrome by, for example, preventing eosinophil production and migration.

In another specific embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention are used to enhance or inhibit complement mediated cell lysis.

In another specific embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention are used to enhance or inhibit antibody dependent cellular cytotoxicity.

In another specific embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention may also be employed for treating atherosclerosis, for example, by preventing monocyte infiltration in the artery wall.

In another specific embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention may be employed to treat adult respiratory distress syndrome (ARDS).

In another specific embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention may be useful for stimulating wound and tissue repair, stimulating angiogenesis, and/or stimulating the repair of vascular or lymphatic diseases or disorders. Additionally, agonists and antagonists of the invention may be used to stimulate the regeneration of mucosal surfaces.

In a specific embodiment, polynucleotides or polypeptides, and/or agonists thereof are used to detect, prevent, diagnose, prognosticate, treat, and/or ameliorate a disorder characterized by primary or acquired immunodeficiency, deficient serum immunoglobulin production, recurrent infections, and/or immune system dysfunction. Moreover, polynucleotides or polypeptides, and/or agonists thereof may be used to treat or prevent infections of the joints, bones, skin, and/or parotid glands, blood-borne infections (e.g., sepsis, meningitis, septic arthritis, and/or osteomyelitis), autoimmune diseases (e.g., those disclosed herein), inflammatory disorders, and malignancies, and/or any disease or disorder or condition associated with these infections, diseases, disorders and/or malignancies) including, but not limited to, CVID, other primary immune deficiencies, HIV disease, CLL, recurrent bronchitis, sinusitis, otitis media, conjunctivitis, pneumonia, hepatitis, meningitis, herpes zoster (e.g., severe herpes zoster), and/or pneumocystis carnii. Other diseases and disorders that may be detected, prevented, diagnosed, prognosticated, treated, and/or ameliorated with polynucleotides or polypeptides, and/or agonists of the present invention include, but are not limited to, HIV infection, HTLV-BLV infection, lymphopenia, phagocyte bactericidal dysfunction anemia, thrombocytopenia, and hemoglobinuria.

In another embodiment, polynucleotides, polypeptides, antibodies, and/or agonists or antagonists of the present invention are used to treat, and/or diagnose an individual having common variable immunodeficiency disease (“CVID”; also known as “acquired agammaglobulinemia” and “acquired hypogammaglobulinemia”) or a subset of this disease.

In a specific embodiment, polynucleotides, polypeptides, antibodies, and/or agonists or antagonists of the present invention may be used to detect, prevent, diagnose, prognosticate, treat, and/or ameliorate cancers or neoplasms including immune cell or immune tissue-related cancers or neoplasms. Examples of cancers or neoplasms that may be detected, prevented, diagnosed, prognosticated, treated, and/or ameliorated by polynucleotides, polypeptides, antibodies, and/or agonists or antagonists of the present invention include, but are not limited to, acute myelogenous leukemia, chronic myelogenous leukemia, Hodgkin's disease, non-Hodgkin's lymphoma, acute lymphocytic anemia (ALL) Chronic lymphocyte leukemia, plasmacytomas, multiple myeloma, Burkitt's lymphoma, EBV-transformed diseases, and/or diseases and disorders described in the section entitled “Hyperproliferative Disorders” elsewhere herein.

In another specific embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention are used as a therapy for decreasing cellular proliferation of Large B-cell Lymphomas.

In another specific embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention are used as a means of decreasing the involvement of B cells and Ig associated with Chronic Myelogenous Leukemia.

In specific embodiments, the compositions of the invention are used as an agent to boost immunoresponsiveness among B cell immunodeficient individuals, such as, for example, an individual who has undergone a partial or complete splenectomy.

Antagonists of the invention include, for example, binding and/or inhibitory antibodies, antisense nucleic acids, ribozymes or soluble forms of the polypeptides of the present invention (e.g., Fc fusion protein; see, e.g., Example 9). Agonists of the invention include, for example, binding or stimulatory antibodies, and soluble forms of the polypeptides (e.g., Fc fusion proteins; see, e.g., Example 9). polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention may be employed in a composition with a pharmaceutically acceptable carrier, e.g., as described herein.

In another embodiment, polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention are administered to an animal (including, but not limited to, those listed above, and also including transgenic animals) incapable of producing functional endogenous antibody molecules or having an otherwise compromised endogenous immune system, but which is capable of producing human immunoglobulin molecules by means of a reconstituted or partially reconstituted immune system from another animal (see, e.g., published PCT Application Nos. WO98/24893, WO/9634096, WO/9633735, and WO/9110741). Administration of polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention to such animals is useful for the generation of monoclonal antibodies against the polypeptides, antibodies, polynucleotides and/or agonists or antagonists of the present invention.

Hyperproliferative Disorders

In certain embodiments, polynucleotides or polypeptides, or agonists or antagonists of the present invention can be used to treat or detect hyperproliferative disorders, including neoplasms. Polynucleotides or polypeptides, or agonists or antagonists of the present invention may inhibit the proliferation of the disorder through direct or indirect interactions. Alternatively, Polynucleotides or polypeptides, or agonists or antagonists of the present invention may proliferate other cells which can inhibit the hyperproliferative disorder.

For example, by increasing an immune response, particularly increasing antigenic qualities of the hyperproliferative disorder or by proliferating, differentiating, or mobilizing T-cells, hyperproliferative disorders can be treated. This immune response may be increased by either enhancing an existing immune response, or by initiating a new immune response. Alternatively, decreasing an immune response may also be a method of treating hyperproliferative disorders, such as a chemotherapeutic agent.

Examples of hyperproliferative disorders that can be treated or detected by polynucleotides or polypeptides, or agonists or antagonists of the present invention include, but are not limited to neoplasms located in the: colon, abdomen, bone, breast, digestive system, liver, pancreas, peritoneum, endocrine glands (adrenal, parathyroid, pituitary, testicles, ovary, thymus, thyroid), eye, head and neck, nervous (central and peripheral), lymphatic system, pelvis, skin, soft tissue, spleen, thorax, and urogenital tract.

Similarly, other hyperproliferative disorders can also be treated or detected by polynucleotides or polypeptides, or agonists or antagonists of the present invention. Examples of such hyperproliferative disorders include, but are not limited to: Acute Childhood Lymphoblastic Leukemia, Acute Lymphoblastic Leukemia, Acute Lymphocytic Leukemia, Acute Myeloid Leukemia, Adrenocortical Carcinoma, Adult (Primary) Hepatocellular Cancer, Adult (Primary) Liver Cancer, Adult Acute Lymphocytic Leukemia, Adult Acute Myeloid Leukemia, Adult Hodgkin's Disease, Adult Hodgkin's Lymphoma, Adult Lymphocytic Leukemia, Adult Non-Hodgkin's Lymphoma, Adult Primary Liver Cancer, Adult Soft Tissue Sarcoma, AIDS-Related Lymphoma, AIDS-Related Malignancies, Anal Cancer, Astrocytoma, Bile Duct Cancer, Bladder Cancer, Bone Cancer, Brain Stem Glioma, Brain Tumors, Breast Cancer, Cancer of the Renal Pelvis and Ureter, Central Nervous System (Primary) Lymphoma, Central Nervous System Lymphoma, Cerebellar Astrocytoma, Cerebral Astrocytoma, Cervical Cancer, Childhood (Primary) Hepatocellular Cancer, Childhood (Primary) Liver Cancer, Childhood Acute Lymphoblastic Leukemia, Childhood Acute Myeloid Leukemia, Childhood Brain Stem Glioma, Childhood Cerebellar Astrocytoma, Childhood Cerebral Astrocytoma, Childhood Extracranial Germ Cell Tumors, Childhood Hodgkin's Disease, Childhood Hodgkin's Lymphoma, Childhood Hypothalamic and Visual Pathway Glioma, Childhood Lymphoblastic Leukemia, Childhood Medulloblastoma, Childhood Non-Hodgkin's Lymphoma, Childhood Pineal and Supratentorial Primitive Neuroectodermal Tumors, Childhood Primary Liver Cancer, Childhood Rhabdomyosarcoma, Childhood Soft Tissue Sarcoma, Childhood Visual Pathway and Hypothalamic Glioma, Chronic Lymphocytic Leukemia, Chronic Myelogenous Leukemia, Colon Cancer, Cutaneous T-Cell Lymphoma, Endocrine Pancreas Islet Cell Carcinoma, Endometrial Cancer, Ependymoma, Epithelial Cancer, Esophageal Cancer, Ewing's Sarcoma and Related Tumors, Exocrine Pancreatic Cancer, Extracranial Germ Cell Tumor, Extragonadal Germ Cell Tumor, Extrahepatic Bile Duct Cancer, Eye Cancer, Female Breast Cancer, Gaucher's Disease, Gallbladder Cancer, Gastric Cancer, Gastrointestinal Carcinoid Tumor, Gastrointestinal Tumors, Germ Cell Tumors, Gestational Trophoblastic Tumor, Hairy Cell Leukemia, Head and Neck Cancer, Hepatocellular Cancer, Hodgkin's Disease, Hodgkin's Lymphoma, Hypergammaglobulinemia, Hypopharyngeal Cancer, Intestinal Cancers, Intraocular Melanoma, Islet Cell Carcinoma, Islet Cell Pancreatic Cancer, Kaposi's Sarcoma, Kidney Cancer, Laryngeal Cancer, Lip and Oral Cavity Cancer, Liver Cancer, Lung Cancer, Lymphoproliferative Disorders, Macroglobulinemia, Male Breast Cancer, Malignant Mesothelioma, Malignant Thymoma, Medulloblastoma, Melanoma, Mesothelioma, Metastatic Occult Primary Squamous Neck Cancer, Metastatic Primary Squamous Neck Cancer, Metastatic Squamous Neck Cancer, Multiple Myeloma, Multiple Myeloma/Plasma Cell Neoplasm, Myelodysplastic Syndrome, Myelogenous Leukemia, Myeloid Leukemia, Myeloproliferative Disorders, Nasal Cavity and Paranasal Sinus Cancer, Nasopharyngeal Cancer, Neuroblastoma, Non-Hodgkin's Lymphoma During Pregnancy, Nonmelanoma Skin Cancer, Non-Small Cell Lung Cancer, Occult Primary Metastatic Squamous Neck Cancer, Oropharyngeal Cancer, Osteo-/Malignant Fibrous Sarcoma, Osteosarcoma/Malignant Fibrous Histiocytoma, Osteosarcoma/Malignant Fibrous Histiocytoma of Bone, Ovarian Epithelial Cancer, Ovarian Germ Cell Tumor, Ovarian Low Malignant Potential Tumor, Pancreatic Cancer, Paraproteinemias, Purpura, Parathyroid Cancer, Penile Cancer, Pheochromocytoma, Pituitary Tumor, Plasma Cell Neoplasm/Multiple Myeloma, Primary Central Nervous System Lymphoma, Primary Liver Cancer, Prostate Cancer, Rectal Cancer, Renal Cell Cancer, Renal Pelvis and Ureter Cancer, Retinoblastoma, Rhabdomyosarcoma, Salivary Gland Cancer, Sarcoidosis Sarcomas, Sezary Syndrome, Skin Cancer, Small Cell Lung Cancer, Small Intestine Cancer, Soft Tissue Sarcoma, Squamous Neck Cancer, Stomach Cancer, Supratentorial Primitive Neuroectodermal and Pineal Tumors, T-Cell Lymphoma, Testicular Cancer, Thymoma, Thyroid Cancer, Transitional Cell Cancer of the Renal Pelvis and Ureter, Transitional Renal Pelvis and Ureter Cancer, Trophoblastic Tumors, Ureter and Renal Pelvis Cell Cancer, Urethral Cancer, Uterine Cancer, Uterine Sarcoma, Vaginal Cancer, Visual Pathway and Hypothalamic Glioma, Vulvar Cancer, Waldenstrom's Macroglobulinemia, Wilms' Tumor, and any other hyperproliferative disease, besides neoplasia, located in an organ system listed above.

In another preferred embodiment, polynucleotides or polypeptides, or agonists or antagonists of the present invention are used to detect, prevent, diagnose, prognosticate, treat, and/or ameliorate premalignant conditions and to prevent progression to a neoplastic or malignant state, including but not limited to those disorders described above. Such uses are indicated in conditions known or suspected of preceding progression to neoplasia or cancer, in particular, where non-neoplastic cell growth consisting of hyperplasia, metaplasia, or most particularly, dysplasia has occurred (for review of such abnormal growth conditions, see Robbins and Angell, 1976, Basic Pathology, 2d Ed., W. B. Saunders Co., Philadelphia, pp. 68-79.)

Hyperplasia is a form of controlled cell proliferation, involving an increase in cell number in a tissue or organ, without significant alteration in structure or function. Hyperplastic disorders which can be detected, prevented, diagnosed, prognosticated, treated, and/or ameliorated with compositions of the invention (including polynucleotides, polypeptides, agonists or antagonists) include, but are not limited to, angiofollicular mediastinal lymph node hyperplasia, angiolymphoid hyperplasia with eosinophilia, atypical melanocytic hyperplasia, basal cell hyperplasia, benign giant lymph node hyperplasia, cementum hyperplasia, congenital adrenal hyperplasia, congenital sebaceous hyperplasia, cystic hyperplasia, cystic hyperplasia of the breast, denture hyperplasia, ductal hyperplasia, endometrial hyperplasia, fibromuscular hyperplasia, focal epithelial hyperplasia, gingival hyperplasia, inflammatory fibrous hyperplasia, inflammatory papillary hyperplasia, intravascular papillary endothelial hyperplasia, nodular hyperplasia of prostate, nodular regenerative hyperplasia, pseudoepitheliomatous hyperplasia, senile sebaceous hyperplasia, and verrucous hyperplasia.

Metaplasia is a form of controlled cell growth in which one type of adult or fully differentiated cell substitutes for another type of adult cell. Metaplastic disorders which can be detected, prevented, diagnosed, prognosticated, treated, and/or ameliorated with compositions of the invention (including polynucleotides, polypeptides, agonists or antagonists) include, but are not limited to, agnogenic myeloid metaplasia, apocrine metaplasia, atypical metaplasia, autoparenchymatous metaplasia, connective tissue metaplasia, epithelial metaplasia, intestinal metaplasia, metaplastic anemia, metaplastic ossification, metaplastic polyps, myeloid metaplasia, primary myeloid metaplasia, secondary myeloid metaplasia, squamous metaplasia, squamous metaplasia of amnion, and symptomatic myeloid metaplasia.

Dysplasia is frequently a forerunner of cancer, and is found mainly in the epithelia; it is the most disorderly form of non-neoplastic cell growth, involving a loss in individual cell uniformity and in the architectural orientation of cells. Dysplastic cells often have abnormally large, deeply stained nuclei, and exhibit pleomorphism. Dysplasia characteristically occurs where there exists chronic irritation or inflammation. Dysplastic disorders which can be detected, prevented, diagnosed, prognosticated, treated, and/or ameliorated with compositions of the invention (including polynucleotides, polypeptides, agonists or antagonists) include, but are not limited to, anhidrotic ectodermal dysplasia, anterofacial dysplasia, asphyxiating thoracic dysplasia, atriodigital dysplasia, bronchopulmonary dysplasia, cerebral dysplasia, cervical dysplasia, chondroectodermal dysplasia, cleidocranial dysplasia, congenital ectodermal dysplasia, craniodiaphysial dysplasia, craniocarpotarsal dysplasia, craniometaphysial dysplasia, dentin dysplasia, diaphysial dysplasia, ectodermal dysplasia, enamel dysplasia, encephalo-ophthalmic dysplasia, dysplasia epiphysialis hemimelia, dysplasia epiphysialis multiplex, dysplasia epiphysialis punctata, epithelial dysplasia, faciodigitogenital dysplasia, familial fibrous dysplasia of jaws, familial white folded dysplasia, fibromuscular dysplasia, fibrous dysplasia of bone, florid osseous dysplasia, hereditary renal-retinal dysplasia, hidrotic ectodermal dysplasia, hypohidrotic ectodermal dysplasia, lymphopenic thymic dysplasia, mammary dysplasia, mandibulofacial dysplasia, metaphysial dysplasia, Mondini dysplasia, monostotic fibrous dysplasia, mucoepithelial dysplasia, multiple epiphysial dysplasia, oculoauriculovertebral dysplasia, oculodentodigital dysplasia, oculovertebral dysplasia, odontogenic dysplasia, opthalmomandibulomelic dysplasia, periapical cemental dysplasia, polyostotic fibrous dysplasia, pseudoachondroplastic spondyloepiphysial dysplasia, retinal dysplasia, septo-optic dysplasia, spondyloepiphysial dysplasia, and ventriculoradial dysplasia.

Additional pre-neoplastic disorders which can be detected, prevented, diagnosed, prognosticated, treated, and/or ameliorated with compositions of the invention (including polynucleotides, polypeptides, agonists or antagonists) include, but are not limited to, benign dysproliferative disorders (e.g., benign tumors, fibrocystic conditions, tissue hypertrophy, intestinal polyps, colon polyps, and esophageal dysplasia), leukoplakia, keratoses, Bowen's disease, Farmer's Skin, solar cheilitis, and solar keratosis.

In another embodiment, a polypeptide of the invention, or polynucleotides, antibodies, agonists, or antagonists corresponding to that polypeptide, may be used to diagnose and/or prognosticate disorders associated with the tissue(s) in which the polypeptide of the invention is expressed, including one, two, three, four, five, or more tissues disclosed in Table 1B.2, column 5 (Tissue Distribution Library Code).

In another embodiment, polynucleotides, polypeptides, antibodies, and/or agonists or antagonists of the present invention conjugated to a toxin or a radioactive isotope, as described herein, may be used to treat cancers and neoplasms, including, but not limited to those described herein. In a further preferred embodiment, polynucleotides, polypeptides, antibodies, and/or agonists or antagonists of the present invention conjugated to a toxin or a radioactive isotope, as described herein, may be used to treat acute myelogenous leukemia.

Additionally, polynucleotides, polypeptides, and/or agonists or antagonists of the invention may affect apoptosis, and therefore, would be useful in treating a number of diseases associated with increased cell survival or the inhibition of apoptosis. For example, diseases associated with increased cell survival or the inhibition of apoptosis that could be detected, prevented, diagnosed, prognosticated, treated, and/or ameliorated by polynucleotides, polypeptides, and/or agonists or antagonists of the invention, include cancers (such as follicular lymphomas, carcinomas with p53 mutations, and hormone-dependent tumors, including, but not limited to colon cancer, cardiac tumors, pancreatic cancer, melanoma, retinoblastoma, glioblastoma, lung cancer, intestinal cancer, testicular cancer, stomach cancer, neuroblastoma, myxoma, myoma, lymphoma, endothelioma, osteoblastoma, osteoclastoma, osteosarcoma, chondrosarcoma, adenoma, breast cancer, prostate cancer, Kaposi's sarcoma and ovarian cancer); autoimmune disorders such as, multiple sclerosis, Sjogren's syndrome, Hashimoto's thyroiditis, biliary cirrhosis, Behcet's disease, Crohn's disease, polymyositis, systemic lupus erythematosus and immune-related glomerulonephritis and rheumatoid arthritis) and viral infections (such as herpes viruses, pox viruses and adenoviruses), inflammation, graft v. host disease, acute graft rejection, and chronic graft rejection.

In preferred embodiments, polynucleotides, polypeptides, and/or agonists or antagonists of the invention are used to inhibit growth, progression, and/or metastasis of cancers, in particular those listed above.

Additional diseases or conditions associated with increased cell survival that could be detected, prevented, diagnosed, prognosticated, treated, and/or ameliorated by polynucleotides, polypeptides, and/or agonists or antagonists of the invention, include, but are not limited to, progression, and/or metastases of malignancies and related disorders such as leukemia (including acute leukemias (e.g., acute lymphocytic leukemia, acute myelocytic leukemia (including myeloblastic, promyelocytic, myelomonocytic, monocytic, and erythroleukemia)) and chronic leukemias (e.g., chronic myelocytic (granulocytic) leukemia and chronic lymphocytic leukemia)), polycythemia vera, lymphomas (e.g., Hodgkin's disease and non-Hodgkin's disease), multiple myeloma, Waldenstrom's macroglobulinemia, heavy chain disease, and solid tumors including, but not limited to, sarcomas and carcinomas such as fibrosarcoma, myxosarcoma, liposarcoma, chondrosarcoma, osteogenic sarcoma, chordoma, angiosarcoma, endotheliosarcoma, lymphangiosarcoma, lymphangioendotheliosarcoma, synovioma, mesothelioma, Ewing's tumor, leiomyosarcoma, rhabdomyosarcoma, colon carcinoma, pancreatic cancer, breast cancer, ovarian cancer, prostate cancer, squamous cell carcinoma, basal cell carcinoma, adenocarcinoma, sweat gland carcinoma, sebaceous gland carcinoma, papillary carcinoma, papillary adenocarcinomas, cystadenocarcinoma, medullary carcinoma, bronchogenic carcinoma, renal cell carcinoma, hepatoma, bile duct carcinoma, choriocarcinoma, seminoma, embryonal carcinoma, Wilm's tumor, cervical cancer, testicular tumor, lung carcinoma, small cell lung carcinoma, bladder carcinoma, epithelial carcinoma, glioma, astrocytoma, medulloblastoma, craniopharyngioma, ependymoma, pinealoma, emangioblastoma, acoustic neuroma, oligodendroglioma, menangioma, melanoma, neuroblastoma, and retinoblastoma.

Diseases associated with increased apoptosis that could be detected, prevented, diagnosed, prognosticated, treated, and/or ameliorated by polynucleotides, polypeptides, and/or agonists or antagonists of the invention, include AIDS; neurodegenerative disorders (such as Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis, retinitis pigmentosa, cerebellar degeneration and brain tumor or prior associated disease); autoimmune disorders (such as, multiple sclerosis, Sjogren's syndrome, Hashimoto's thyroiditis, biliary cirrhosis, Behcet's disease, Crohn's disease, polymyositis, systemic lupus erythematosus and immune-related glomerulonephritis and rheumatoid arthritis) myelodysplastic syndromes (such as aplastic anemia), graft v. host disease, ischemic injury (such as that caused by myocardial infarction, stroke and reperfusion injury), liver injury (e.g., hepatitis related liver injury, ischemia/reperfusion injury, cholestosis (bile duct injury) and liver cancer); toxin-induced liver disease (such as that caused by alcohol), septic shock, cachexia and anorexia.

Hyperproliferative diseases and/or disorders that could be detected, prevented, diagnosed, prognosticated, treated, and/or ameliorated by polynucleotides, polypeptides, and/or agonists or antagonists of the invention, include, but are not limited to, neoplasms located in the liver, abdomen, bone, breast, digestive system, pancreas, peritoneum, endocrine glands (adrenal, parathyroid, pituitary, testicles, ovary, thymus, thyroid), eye, head and neck, nervous system (central and peripheral), lymphatic system, pelvis, skin, soft tissue, spleen, thorax, and urogenital tract.

Similarly, other hyperproliferative disorders can also be detected, prevented, diagnosed, prognosticated, treated, and/or ameliorated by polynucleotides, polypeptides, and/or agonists or antagonists of the invention. Examples of such hyperproliferative disorders include, but are not limited to: hypergammaglobulinemia, lymphoproliferative disorders, paraproteinemias, purpura, sarcoidosis, Sezary Syndrome, Waldenstron's macroglobulinemia, Gaucher's Disease, histiocytosis, and any other hyperproliferative disease, besides neoplasia, located in an organ system listed above.

Another preferred embodiment utilizes polynucleotides of the present invention to inhibit aberrant cellular division, by gene therapy using the present invention, and/or protein fusions or fragments thereof.

Thus, the present invention provides a method for treating cell proliferative disorders by inserting into an abnormally proliferating cell a polynucleotide of the present invention, wherein said polynucleotide represses said expression.

Another embodiment of the present invention provides a method of treating cell-proliferative disorders in individuals comprising administration of one or more active gene copies of the present invention to an abnormally proliferating cell or cells. In a preferred embodiment, polynucleotides of the present invention is a DNA construct comprising a recombinant expression vector effective in expressing a DNA sequence encoding said polynucleotides. In another preferred embodiment of the present invention, the DNA construct encoding the polynucleotides of the present invention is inserted into cells to be treated utilizing a retrovirus, or more preferably an adenoviral vector (See G J. Nabel, et. al., PNAS 1999 96: 324-326, which is hereby incorporated by reference). In a most preferred embodiment, the viral vector is defective and will not transform non-proliferating cells, only proliferating cells. Moreover, in a preferred embodiment, the polynucleotides of the present invention inserted into proliferating cells either alone, or in combination with or fused to other polynucleotides, can then be modulated via an external stimulus (i.e. magnetic, specific small molecule, chemical, or drug administration, etc.), which acts upon the promoter upstream of said polynucleotides to induce expression of the encoded protein product. As such the beneficial therapeutic affect of the present invention may be expressly modulated (i.e. to increase, decrease, or inhibit expression of the present invention) based upon said external stimulus.

Polynucleotides of the present invention may be useful in repressing expression of oncogenic genes or antigens. By “repressing expression of the oncogenic genes” is intended the suppression of the transcription of the gene, the degradation of the gene transcript (pre-message RNA), the inhibition of splicing, the destruction of the messenger RNA, the prevention of the post-translational modifications of the protein, the destruction of the protein, or the inhibition of the normal function of the protein.

For local administration to abnormally proliferating cells, polynucleotides of the present invention may be administered by any method known to those of skill in the art including, but not limited to transfection, electroporation, microinjection of cells, or in vehicles such as liposomes, LIPOFECTIN™, or as naked polynucleotides, or any other method described throughout the specification. The polynucleotide of the present invention may be delivered by known gene delivery systems such as, but not limited to, retroviral vectors (Gilboa, J. Virology 44:845 (1982); Hocke, Nature 320:275 (1986); Wilson, et al., Proc. Natl. Acad. Sci. U.S.A. 85:3014), vaccinia virus system (Chakrabarty et al., Mol. Cell. Biol. 5:3403 (1985) or other efficient DNA delivery systems (Yates et al., Nature 313:812 (1985)) known to those skilled in the art. These references are exemplary only and are hereby incorporated by reference. In order to specifically deliver or transfect cells which are abnormally proliferating and spare non-dividing cells, it is preferable to utilize a retrovirus, or adenoviral (as described in the art and elsewhere herein) delivery system known to those of skill in the art. Since host DNA replication is required for retroviral DNA to integrate and the retrovirus will be unable to self replicate due to the lack of the retrovirus genes needed for its life cycle. Utilizing such a retroviral delivery system for polynucleotides of the present invention will target said gene and constructs to abnormally proliferating cells and will spare the non-dividing normal cells.

The polynucleotides of the present invention may be delivered directly to cell proliferative disorder/disease sites in internal organs, body cavities and the like by use of imaging devices used to guide an injecting needle directly to the disease site. The polynucleotides of the present invention may also be administered to disease sites at the time of surgical intervention.

By “cell proliferative disease” is meant any human or animal disease or disorder, affecting any one or any combination of organs, cavities, or body parts, which is characterized by single or multiple local abnormal proliferations of cells, groups of cells, or tissues, whether benign or malignant.

Any amount of the polynucleotides of the present invention may be administered as long as it has a biologically inhibiting effect on the proliferation of the treated cells. Moreover, it is possible to administer more than one of the polynucleotide of the present invention simultaneously to the same site. By “biologically inhibiting” is meant partial or total growth inhibition as well as decreases in the rate of proliferation or growth of the cells. The biologically inhibitory dose may be determined by assessing the effects of the polynucleotides of the present invention on target malignant or abnormally proliferating cell growth in tissue culture, tumor growth in animals and cell cultures, or any other method known to one of ordinary skill in the art.

The present invention is further directed to antibody-based therapies which involve administering of anti-polypeptides and anti-polynucleotide antibodies to a mammalian, preferably human, patient for treating one or more of the described disorders. Methods for producing anti-polypeptides and anti-polynucleotide antibodies polyclonal and monoclonal antibodies are described in detail elsewhere herein. Such antibodies may be provided in pharmaceutically acceptable compositions as known in the art or as described herein.

A summary of the ways in which the antibodies of the present invention may be used therapeutically includes binding polynucleotides or polypeptides of the present invention locally or systemically in the body or by direct cytotoxicity of the antibody, e.g. as mediated by complement (CDC) or by effector cells (ADCC). Some of these approaches are described in more detail below. Armed with the teachings provided herein, one of ordinary skill in the art will know how to use the antibodies of the present invention for diagnosis, prognosis, monitoring, or therapeutic purposes without undue experimentation.

In particular, the antibodies, fragments and derivatives of the present invention are useful for treating a subject having or developing cell proliferative and/or differentiation disorders as described herein. Such treatment comprises administering a single or multiple doses of the antibody, or a fragment, derivative, or a conjugate thereof.

The antibodies of this invention may be advantageously utilized in combination with other monoclonal or chimeric antibodies, or with lymphokines or hematopoietic growth factors, for example, which serve to increase the number or activity of effector cells which interact with the antibodies.

It is preferred to use high affinity and/or potent in vivo inhibiting and/or neutralizing antibodies against polypeptides or polynucleotides of the present invention, fragments or regions thereof, for both immunoassays directed to and therapy of disorders related to polynucleotides or polypeptides, including fragments thereof, of the present invention. Such antibodies, fragments, or regions, will preferably have an affinity for polynucleotides or polypeptides, including fragments thereof. Preferred binding affinities include those with a dissociation constant or Kd less than 5×10⁻⁶M, 10⁻⁶M, 5×10⁻⁷M, 10⁻⁷M, 5×10⁻⁸M, 10⁻⁸M, 5×10⁻⁹M, 10⁻⁹M, 5×10⁻¹⁰M, 10⁻¹⁰ M, 5×10⁻¹¹M, 10⁻¹¹M, 5×10⁻¹²M, 10⁻¹²M, 5×10⁻¹³M, 10⁻¹³M, 5×10⁻¹⁴M, 10⁻¹⁴M, 5×10⁻¹⁵M, and 10⁻¹⁵M.

Moreover, polypeptides of the present invention are useful in inhibiting the angiogenesis of proliferative cells or tissues, either alone, as a protein fusion, or in combination with other polypeptides directly or indirectly, as described elsewhere herein. In a most preferred embodiment, said anti-angiogenesis effect may be achieved indirectly, for example, through the inhibition of hematopoietic, tumor-specific cells, such as tumor-associated macrophages (See Joseph I B, et al. J Natl Cancer Inst, 90(21):1648-53 (1998), which is hereby incorporated by reference). Antibodies directed to polypeptides or polynucleotides of the present invention may also result in inhibition of angiogenesis directly, or indirectly (See Witte L, et al., Cancer Metastasis Rev. 17(2):155-61 (1998), which is hereby incorporated by reference)).

Polypeptides, including protein fusions, of the present invention, or fragments thereof may be useful in inhibiting proliferative cells or tissues through the induction of apoptosis. Said polypeptides may act either directly, or indirectly to induce apoptosis of proliferative cells and tissues, for example in the activation of a death-domain receptor, such as tumor necrosis factor (TNF) receptor-1, CD95 (Fas/APO-1), TNF-receptor-related apoptosis-mediated protein (TRAMP) and TNF-related apoptosis-inducing ligand (TRAIL) receptor-1 and -2 (See Schulze-Osthoff K, et. al., Eur J Biochem 254(3):439-59 (1998), which is hereby incorporated by reference). Moreover, in another preferred embodiment of the present invention, said polypeptides may induce apoptosis through other mechanisms, such as in the activation of other proteins which will activate apoptosis, or through stimulating the expression of said proteins, either alone or in combination with small molecule drugs or adjuvants, such as apoptonin, galectins, thioredoxins, anti-inflammatory proteins (See for example, Mutat Res 400(1-2):447-55 (1998), Med. Hypotheses.50(5):423-33 (1998), Chem Biol Interact. Apr 24; 111-112:23-34 (1998), J Mol. Med. 76(6):402-12 (1998), Int J Tissue React; 20(1):3-15 (1998), which are all hereby incorporated by reference).

Polypeptides, including protein fusions to, or fragments thereof, of the present invention are useful in inhibiting the metastasis of proliferative cells or tissues. Inhibition may occur as a direct result of administering polypeptides, or antibodies directed to said polypeptides as described elsewhere herein, or indirectly, such as activating the expression of proteins known to inhibit metastasis, for example alpha 4 integrins, (See, e.g., Curr Top Microbiol Immunol 1998; 231:125-41, which is hereby incorporated by reference). Such therapeutic affects of the present invention may be achieved either alone, or in combination with small molecule drugs or adjuvants.

In another embodiment, the invention provides a method of delivering compositions containing the polypeptides of the invention (e.g., compositions containing polypeptides or polypeptide antibodies associated with heterologous polypeptides, heterologous nucleic acids, toxins, or prodrugs) to targeted cells expressing the polypeptide of the present invention. Polypeptides or polypeptide antibodies of the invention may be associated with heterologous polypeptides, heterologous nucleic acids, toxins, or prodrugs via hydrophobic, hydrophilic, ionic and/or covalent interactions.

Polypeptides, protein fusions to, or fragments thereof, of the present invention are useful in enhancing the immunogenicity and/or antigenicity of proliferating cells or tissues, either directly, such as would occur if the polypeptides of the present invention ‘vaccinated’ the immune response to respond to proliferative antigens and immunogens, or indirectly, such as in activating the expression of proteins known to enhance the immune response (e.g. chemokines), to said antigens and immunogens.

Anti-Angiogenesis Activity

The naturally occurring balance between endogenous stimulators and inhibitors of angiogenesis is one in which inhibitory influences predominate. Rastinejad et al., Cell 56:345-355 (1989). In those rare instances in which neovascularization occurs under normal physiological conditions, such as wound healing, organ regeneration, embryonic development, and female reproductive processes, angiogenesis is stringently regulated and spatially and temporally delimited. Under conditions of pathological angiogenesis such as that characterizing solid tumor growth, these regulatory controls fail. Unregulated angiogenesis becomes pathologic and sustains progression of many neoplastic and non-neoplastic diseases. A number of serious diseases are dominated by abnormal neovascularization including solid tumor growth and metastases, arthritis, some types of eye disorders, and psoriasis. See, e.g., reviews by Moses et al., Biotech. 9:630-634 (1991); Folkman et al., N. Engl J. Med., 333:1757-1763 (1995); Auerbach et al., J. Microvasc. Res. 29:401-411 (1985); Folkman, Advances in Cancer Research, eds. Klein and Weinhouse, Academic Press, New York, pp. 175-203 (1985); Patz, Am. J. Opthalmol 94:715-743 (1982); and Folkman et al., Science 221:719-725 (1983). In a number of pathological conditions, the process of angiogenesis contributes to the disease state. For example, significant data have accumulated which suggest that the growth of solid tumors is dependent on angiogenesis. Folkman and Klagsbrun, Science 235:442-447 (1987).

The present invention provides for treatment of diseases or disorders associated with neovascularization by administration of the polynucleotides and/or polypeptides of the invention, as well as agonists or antagonists of the present invention. Malignant and metastatic conditions which can be treated with the polynucleotides and polypeptides, or agonists or antagonists of the invention include, but are not limited to, malignancies, solid tumors, and cancers described herein and otherwise known in the art (for a review of such disorders, see Fishman et al., Medicine, 2d Ed., J. B. Lippincott Co., Philadelphia (1985)).Thus, the present invention provides a method of treating an angiogenesis-related disease and/or disorder, comprising administering to an individual in need thereof a therapeutically effective amount of a polynucleotide, polypeptide, antagonist and/or agonist of the invention. For example, polynucleotides, polypeptides, antagonists and/or agonists may be utilized in a variety of additional methods in order to therapeutically treat a cancer or tumor. Cancers which may be treated with polynucleotides, polypeptides, antagonists and/or agonists include, but are not limited to solid tumors, including prostate, lung, breast, ovarian, stomach, pancreas, larynx, esophagus, testes, liver, parotid, biliary tract, colon, rectum, cervix, uterus, endometrium, kidney, bladder, thyroid cancer; primary tumors and metastases; melanomas; glioblastoma; Kaposi's sarcoma; leiomyosarcoma; non-small cell lung cancer; colorectal cancer; advanced malignancies; and blood born tumors such as leukemias. For example, polynucleotides, polypeptides, antagonists and/or agonists may be delivered topically, in order to treat cancers such as skin cancer, head and neck tumors, breast tumors, and Kaposi's sarcoma.

Within yet other aspects, polynucleotides, polypeptides, antagonists and/or agonists may be utilized to treat superficial forms of bladder cancer by, for example, intravesical administration. Polynucleotides, polypeptides, antagonists and/or agonists may be delivered directly into the tumor, or near the tumor site, via injection or a catheter. Of course, as the artisan of ordinary skill will appreciate, the appropriate mode of administration will vary according to the cancer to be treated. Other modes of delivery are discussed herein.

Polynucleotides, polypeptides, antagonists and/or agonists may be useful in treating other disorders, besides cancers, which involve angiogenesis. These disorders include, but are not limited to: benign tumors, for example hemangiomas, acoustic neuromas, neurofibromas, trachomas, and pyogenic granulomas; artheroscleric plaques; ocular angiogenic diseases, for example, diabetic retinopathy, retinopathy of prematurity, macular degeneration, corneal graft rejection, neovascular glaucoma, retrolental fibroplasia, rubeosis, retinoblastoma, uvietis and Pterygia (abnormal blood vessel growth) of the eye; rheumatoid arthritis; psoriasis; delayed wound healing; endometriosis; vasculogenesis; granulations; hypertrophic scars (keloids); nonunion fractures; scleroderma; trachoma; vascular adhesions; myocardial angiogenesis; coronary collaterals; cerebral collaterals; arteriovenous malformations; ischemic limb angiogenesis; Osler-Webber Syndrome; plaque neovascularization; telangiectasia; hemophiliac joints; angiofibroma; fibromuscular dysplasia; wound granulation; Crohn's disease; and atherosclerosis.

For example, within one aspect of the present invention methods are provided for treating hypertrophic scars and keloids, comprising the step of administering a polynucleotide, polypeptide, antagonist and/or agonist of the invention to a hypertrophic scar or keloid.

Within one embodiment of the present invention polynucleotides, polypeptides, antagonists and/or agonists of the invention are directly injected into a hypertrophic scar or keloid, in order to prevent the progression of these lesions. This therapy is of particular value in the prophylactic treatment of conditions which are known to result in the development of hypertrophic scars and keloids (e.g., burns), and is preferably initiated after the proliferative phase has had time to progress (approximately 14 days after the initial injury), but before hypertrophic scar or keloid development. As noted above, the present invention also provides methods for treating neovascular diseases of the eye, including for example, corneal neovascularization, neovascular glaucoma, proliferative diabetic retinopathy, retrolental fibroplasia and macular degeneration.

Moreover, Ocular disorders associated with neovascularization which can be treated with the polynucleotides and polypeptides of the present invention (including agonists and/or antagonists) include, but are not limited to: neovascular glaucoma, diabetic retinopathy, retinoblastoma, retrolental fibroplasia, uveitis, retinopathy of prematurity macular degeneration, corneal graft neovascularization, as well as other eye inflammatory diseases, ocular tumors and diseases associated with choroidal or iris neovascularization. See, e.g., reviews by Waltman et al., Am. J. Ophthal 85:704-710 (1978) and Gartner et al., Surv. Ophthal 22:291-312 (1978).

Thus, within one aspect of the present invention methods are provided for treating neovascular diseases of the eye such as corneal neovascularization (including corneal graft neovascularization), comprising the step of administering to a patient a therapeutically effective amount of a compound (as described above) to the cornea, such that the formation of blood vessels is inhibited. Briefly, the cornea is a tissue which normally lacks blood vessels. In certain pathological conditions however, capillaries may extend into the cornea from the pericorneal vascular plexus of the limbus. When the cornea becomes vascularized, it also becomes clouded, resulting in a decline in the patient's visual acuity. Visual loss may become complete if the cornea completely opacitates. A wide variety of disorders can result in corneal neovascularization, including for example, corneal infections (e.g., trachoma, herpes simplex keratitis, leishmaniasis and onchocerciasis), immunological processes (e.g., graft rejection and Stevens-Johnson's syndrome), alkali burns, trauma, inflammation (of any cause), toxic and nutritional deficiency states, and as a complication of wearing contact lenses.

Within particularly preferred embodiments of the invention, may be prepared for topical administration in saline (combined with any of the preservatives and antimicrobial agents commonly used in ocular preparations), and administered in eyedrop form. The solution or suspension may be prepared in its pure form and administered several times daily. Alternatively, anti-angiogenic compositions, prepared as described above, may also be administered directly to the cornea. Within preferred embodiments, the anti-angiogenic composition is prepared with a muco-adhesive polymer which binds to cornea. Within further embodiments, the anti-angiogenic factors or anti-angiogenic compositions may be utilized as an adjunct to conventional steroid therapy. Topical therapy may also be useful prophylactically in corneal lesions which are known to have a high probability of inducing an angiogenic response (such as chemical burns). In these instances the treatment, likely in combination with steroids, may be instituted immediately to help prevent subsequent complications.

Within other embodiments, the compounds described above may be injected directly into the corneal stroma by an ophthalmologist under microscopic guidance. The preferred site of injection may vary with the morphology of the individual lesion, but the goal of the administration would be to place the composition at the advancing front of the vasculature (i.e., interspersed between the blood vessels and the normal cornea). In most cases this would involve perilimbic corneal injection to “protect” the cornea from the advancing blood vessels. This method may also be utilized shortly after a corneal insult in order to prophylactically prevent corneal neovascularization. In this situation the material could be injected in the perilimbic cornea interspersed between the corneal lesion and its undesired potential limbic blood supply. Such methods may also be utilized in a similar fashion to prevent capillary invasion of transplanted corneas. In a sustained-release form injections might only be required 2-3 times per year. A steroid could also be added to the injection solution to reduce inflammation resulting from the injection itself.

Within another aspect of the present invention, methods are provided for treating neovascular glaucoma, comprising the step of administering to a patient a therapeutically effective amount of a polynucleotide, polypeptide, antagonist and/or agonist to the eye, such that the formation of blood vessels is inhibited. In one embodiment, the compound may be administered topically to the eye in order to treat early forms of neovascular glaucoma. Within other embodiments, the compound may be implanted by injection into the region of the anterior chamber angle. Within other embodiments, the compound may also be placed in any location such that the compound is continuously released into the aqueous humor. Within another aspect of the present invention, methods are provided for treating proliferative diabetic retinopathy, comprising the step of administering to a patient a therapeutically effective amount of a polynucleotide, polypeptide, antagonist and/or agonist to the eyes, such that the formation of blood vessels is inhibited.

Within particularly preferred embodiments of the invention, proliferative diabetic retinopathy may be treated by injection into the aqueous humor or the vitreous, in order to increase the local concentration of the polynucleotide, polypeptide, antagonist and/or agonist in the retina. Preferably, this treatment should be initiated prior to the acquisition of severe disease requiring photocoagulation.

Within another aspect of the present invention, methods are provided for treating retrolental fibroplasia, comprising the step of administering to a patient a therapeutically effective amount of a polynucleotide, polypeptide, antagonist and/or agonist to the eye, such that the formation of blood vessels is inhibited. The compound may be administered topically, via intravitreous injection and/or via intraocular implants.

Additionally, disorders which can be treated with the polynucleotides, polypeptides, agonists and/or agonists include, but are not limited to, hemangioma, arthritis, psoriasis, angiofibroma, atherosclerotic plaques, delayed wound healing, granulations, hemophilic joints, hypertrophic scars, nonunion fractures, Osler-Weber syndrome, pyogenic granuloma, scleroderma, trachoma, and vascular adhesions.

Moreover, disorders and/or states, which can be detected, prevented, diagnosed, prognosticated, treated, and/or ameliorated with the polynucleotides, polypeptides, agonists and/or agonists of the invention include, but are not limited to, solid tumors, blood born tumors such as leukemias, tumor metastasis, Kaposi's sarcoma, benign tumors, for example hemangiomas, acoustic neuromas, neurofibromas, trachomas, and pyogenic granulomas, rheumatoid arthritis, psoriasis, ocular angiogenic diseases, for example, diabetic retinopathy, retinopathy of prematurity, macular degeneration, corneal graft rejection, neovascular glaucoma, retrolental fibroplasia, rubeosis, retinoblastoma, and uvietis, delayed wound healing, endometriosis, vascluogenesis, granulations, hypertrophic scars (keloids), nonunion fractures, scleroderma, trachoma, vascular adhesions, myocardial angiogenesis, coronary collaterals, cerebral collaterals, arteriovenous malformations, ischemic limb angiogenesis, Osler-Webber Syndrome, plaque neovascularization, telangiectasia, hemophiliac joints, angiofibroma fibromuscular dysplasia, wound granulation, Crohn's disease, atherosclerosis, birth control agent by preventing vascularization required for embryo implantation controlling menstruation, diseases that have angiogenesis as a pathologic consequence such as cat scratch disease (Rochele minalia quintosa), ulcers (Helicobacter pylori), Bartonellosis and bacillary angiomatosis.

In one aspect of the birth control method, an amount of the compound sufficient to block embryo implantation is administered before or after intercourse and fertilization have occurred, thus providing an effective method of birth control, possibly a “morning after” method. Polynucleotides, polypeptides, agonists and/or agonists may also be used in controlling menstruation or administered as either a peritoneal lavage fluid or for peritoneal implantation in the treatment of endometriosis.

Polynucleotides, polypeptides, agonists and/or agonists of the present invention may be incorporated into surgical sutures in order to prevent stitch granulomas.

Polynucleotides, polypeptides, agonists and/or agonists may be utilized in a wide variety of surgical procedures. For example, within one aspect of the present invention a compositions (in the form of, for example, a spray or film) may be utilized to coat or spray an area prior to removal of a tumor, in order to isolate normal surrounding tissues from malignant tissue, and/or to prevent the spread of disease to surrounding tissues. Within other aspects of the present invention, compositions (e.g., in the form of a spray) may be delivered via endoscopic procedures in order to coat tumors, or inhibit angiogenesis in a desired locale. Within yet other aspects of the present invention, surgical meshes which have been coated with anti-angiogenic compositions of the present invention may be utilized in any procedure wherein a surgical mesh might be utilized. For example, within one embodiment of the invention a surgical mesh laden with an anti-angiogenic composition may be utilized during abdominal cancer resection surgery (e.g., subsequent to colon resection) in order to provide support to the structure, and to release an amount of the anti-angiogenic factor.

Within further aspects of the present invention, methods are provided for treating tumor excision sites, comprising administering a polynucleotide, polypeptide, agonist and/or agonist to the resection margins of a tumor subsequent to excision, such that the local recurrence of cancer and the formation of new blood vessels at the site is inhibited. Within one embodiment of the invention, the anti-angiogenic compound is administered directly to the tumor excision site (e.g., applied by swabbing, brushing or otherwise coating the resection margins of the tumor with the anti-angiogenic compound). Alternatively, the anti-angiogenic compounds may be incorporated into known surgical pastes prior to administration. Within particularly preferred embodiments of the invention, the anti-angiogenic compounds are applied after hepatic resections for malignancy, and after neurosurgical operations.

Within one aspect of the present invention, polynucleotides, polypeptides, agonists and/or agonists may be administered to the resection margin of a wide variety of tumors, including for example, breast, colon, brain and hepatic tumors. For example, within one embodiment of the invention, anti-angiogenic compounds may be administered to the site of a neurological tumor subsequent to excision, such that the formation of new blood vessels at the site are inhibited.

The polynucleotides, polypeptides, agonists and/or agonists of the present invention may also be administered along with other anti-angiogenic factors. Representative examples of other anti-angiogenic factors include: Anti-Invasive Factor, retinoic acid and derivatives thereof, paclitaxel, Suramin, Tissue Inhibitor of Metalloproteinase-1, Tissue Inhibitor of Metalloproteinase-2, Plasminogen Activator Inhibitor-1, Plasminogen Activator Inhibitor-2, and various forms of the lighter “d group” transition metals.

Lighter “d group” transition metals include, for example, vanadium, molybdenum, tungsten, titanium, niobium, and tantalum species. Such transition metal species may form transition metal complexes. Suitable complexes of the above-mentioned transition metal species include oxo transition metal complexes.

Representative examples of vanadium complexes include oxo vanadium complexes such as vanadate and vanadyl complexes. Suitable vanadate complexes include metavanadate and orthovanadate complexes such as, for example, ammonium metavanadate, sodium metavanadate, and sodium orthovanadate. Suitable vanadyl complexes include, for example, vanadyl acetylacetonate and vanadyl sulfate including vanadyl sulfate hydrates such as vanadyl sulfate mono- and trihydrates.

Representative examples of tungsten and molybdenum complexes also include oxo complexes. Suitable oxo tungsten complexes include tungstate and tungsten oxide complexes. Suitable tungstate complexes include ammonium tungstate, calcium tungstate, sodium tungstate dihydrate, and tungstic acid. Suitable tungsten oxides include tungsten (IV) oxide and tungsten (VI) oxide. Suitable oxo molybdenum complexes include molybdate, molybdenum oxide, and molybdenyl complexes. Suitable molybdate complexes include ammonium molybdate and its hydrates, sodium molybdate and its hydrates, and potassium molybdate and its hydrates. Suitable molybdenum oxides include molybdenum (VI) oxide, molybdenum (VI) oxide, and molybdic acid. Suitable molybdenyl complexes include, for example, molybdenyl acetylacetonate. Other suitable tungsten and molybdenum complexes include hydroxo derivatives derived from, for example, glycerol, tartaric acid, and sugars.

A wide variety of other anti-angiogenic factors may also be utilized within the context of the present invention. Representative examples include platelet factor 4; protamine sulphate; sulphated chitin derivatives (prepared from queen crab shells), (Murata et al., Cancer Res. 51:22-26, 1991); Sulphated Polysaccharide Peptidoglycan Complex (SP-PG) (the function of this compound may be enhanced by the presence of steroids such as estrogen, and tamoxifen citrate); Staurosporine; modulators of matrix metabolism, including for example, proline analogs, cishydroxyproline, d,L-3,4-dehydroproline, Thiaproline, alpha,alpha-dipyridyl, aminopropionitrile fumarate; 4-propyl-5-(4-pyridinyl)-2(3H)-oxazolone; Methotrexate; Mitoxantrone; Heparin; Interferons; 2 Macroglobulin-serum; ChIMP-3 (Pavloff et al., J. Bio. Chem. 267:17321-17326, 1992); Chymostatin (Tomkinson et al., Biochem J. 286:475-480, 1992); Cyclodextrin Tetradecasulfate; Eponemycin; Camptothecin; Fumagillin (Ingber et al., Nature 348:555-557, 1990); Gold Sodium Thiomalate (“GST”; Matsubara and Ziff, J. Clin. Invest. 79:1440-1446, 1987); anticollagenase-serum; alpha2-antiplasmin (Holmes et al., J. Biol. Chem. 262(4):1659-1664, 1987); Bisantrene (National Cancer Institute); Lobenzarit disodium (N-(2)-carboxyphenyl-4-chloroanthronilic acid disodium or “CCA”; Takeuchi et al., Agents Actions 36:312-316, 1992); Thalidomide; Angostatic steroid; AGM-1470; carboxynaminolmidazole; and metalloproteinase inhibitors such as BB94.

Diseases at the Cellular Level

Diseases associated with increased cell survival or the inhibition of apoptosis that could be detected, prevented, diagnosed, prognosticated, treated, and/or ameliorated using polynucleotides or polypeptides, as well as antagonists or agonists of the present invention, include cancers (such as follicular lymphomas, carcinomas with p53 mutations, and hormone-dependent tumors, including, but not limited to colon cancer, cardiac tumors, pancreatic cancer, melanoma, retinoblastoma, glioblastoma, lung cancer, intestinal cancer, testicular cancer, stomach cancer, neuroblastoma, myxoma, myoma, lymphoma, endothelioma, osteoblastoma, osteoclastoma, osteosarcoma, chondrosarcoma, adenoma, breast cancer, prostate cancer, Kaposi's sarcoma and ovarian cancer); autoimmune disorders (such as, multiple sclerosis, Sjogren's syndrome, Hashimoto's thyroiditis, biliary cirrhosis, Behcet's disease, Crohn's disease, polymyositis, systemic lupus erythematosus and immune-related glomerulonephritis and rheumatoid arthritis) and viral infections (such as herpes viruses, pox viruses and adenoviruses), inflammation, graft v. host disease, acute graft rejection, and chronic graft rejection.

In preferred embodiments, polynucleotides, polypeptides, and/or antagonists of the invention are used to inhibit growth, progression, and/or metasis of cancers, in particular those listed above.

Additional diseases or conditions associated with increased cell survival that could be treated or detected by polynucleotides or polypeptides, or agonists or antagonists of the present invention include, but are not limited to, progression, and/or metastases of malignancies and related disorders such as leukemia (including acute leukemias (e.g., acute lymphocytic leukemia, acute myelocytic leukemia (including myeloblastic, promyelocytic, myelomonocytic, monocytic, and erythroleukemia)) and chronic leukemias (e.g., chronic myelocytic (granulocytic) leukemia and chronic lymphocytic leukemia)), polycythemia vera, lymphomas (e.g., Hodgkin's disease and non-Hodgkin's disease), multiple myeloma, Waldenstrom's macroglobulinemia, heavy chain disease, and solid tumors including, but not limited to, sarcomas and carcinomas such as fibrosarcoma, myxosarcoma, liposarcoma, chondrosarcoma, osteogenic sarcoma, chordoma, angiosarcoma, endotheliosarcoma, lymphangiosarcoma, lymphangioendotheliosarcoma, synovioma, mesothelioma, Ewing's tumor, leiomyosarcoma, rhabdomyosarcoma, colon carcinoma, pancreatic cancer, breast cancer, ovarian cancer, prostate cancer, squamous cell carcinoma, basal cell carcinoma, adenocarcinoma, sweat gland carcinoma, sebaceous gland carcinoma, papillary carcinoma, papillary adenocarcinomas, cystadenocarcinoma, medullary carcinoma, bronchogenic carcinoma, renal cell carcinoma, hepatoma, bile duct carcinoma, choriocarcinoma, seminoma, embryonal carcinoma, Wilm's tumor, cervical cancer, testicular tumor, lung carcinoma, small cell lung carcinoma, bladder carcinoma, epithelial carcinoma, glioma, astrocytoma, medulloblastoma, craniopharyngioma, ependymoma, pinealoma, hemangioblastoma, acoustic neuroma, oligodendroglioma, menangioma, melanoma, neuroblastoma, and retinoblastoma.

Diseases associated with increased apoptosis that could be detected, prevented, diagnosed, prognosticated, treated, and/or ameliorated using polynucleotides or polypeptides, as well as agonists or antagonists of the present invention, include, but are not limited to, AIDS; neurodegenerative disorders (such as Alzheimer's disease, Parkinson's disease, Amyotrophic lateral sclerosis, Retinitis pigmentosa, Cerebellar degeneration and brain tumor or prior associated disease); autoimmune disorders (such as, multiple sclerosis, Sjogren's syndrome, Hashimoto's thyroiditis, biliary cirrhosis, Behcet's disease, Crohn's disease, polymyositis, systemic lupus erythematosus and immune-related glomerulonephritis and rheumatoid arthritis) myelodysplastic syndromes (such as aplastic anemia), graft v. host disease, ischemic injury (such as that caused by myocardial infarction, stroke and reperfusion injury), liver injury (e.g., hepatitis related liver injury, ischemia/reperfusion injury, cholestosis (bile duct injury) and liver cancer); toxin-induced liver disease (such as that caused by alcohol), septic shock, cachexia and anorexia.

Wound Healing and Epithelial Cell Proliferation

In accordance with yet a further aspect of the present invention, there is provided a process for utilizing polynucleotides or polypeptides, as well as agonists or antagonists of the present invention, for therapeutic purposes, for example, to stimulate epithelial cell proliferation and basal keratinocytes for the purpose of wound healing, and to stimulate hair follicle production and healing of dermal wounds. Polynucleotides or polypeptides, as well as agonists or antagonists of the present invention, may be clinically useful in stimulating wound healing including surgical wounds, excisional wounds, deep wounds involving damage of the dermis and epidermis, eye tissue wounds, dental tissue wounds, oral cavity wounds, diabetic ulcers, dermal ulcers, cubitus ulcers, arterial ulcers, venous stasis ulcers, burns resulting from heat exposure or chemicals, and other abnormal wound healing conditions such as uremia, malnutrition, vitamin deficiencies and complications associated with systemic treatment with steroids, radiation therapy and antineoplastic drugs and antimetabolites. Polynucleotides or polypeptides, as well as agonists or antagonists of the present invention, could be used to promote dermal reestablishment subsequent to dermal loss Polynucleotides or polypeptides, as well as agonists or antagonists of the present invention, could be used to increase the adherence of skin grafts to a wound bed and to stimulate re-epithelialization from the wound bed. The following are types of grafts that polynucleotides or polypeptides, agonists or antagonists of the present invention, could be used to increase adherence to a wound bed: autografts, artificial skin, allografts, autodermic graft, autoepdermic grafts, avacular grafts, Blair-Brown grafts, bone graft, brephoplastic grafts, cutis graft, delayed graft, dermic graft, epidermic graft, fascia graft, full thickness graft, heterologous graft, xenograft, homologous graft, hyperplastic graft, lamellar graft, mesh graft, mucosal graft, Ollier-Thiersch graft, omenpal graft, patch graft, pedicle graft, penetrating graft, split skin graft, thick split graft. Polynucleotides or polypeptides, as well as agonists or antagonists of the present invention, can be used to promote skin strength and to improve the appearance of aged skin.

It is believed that polynucleotides or polypeptides, as well as agonists or antagonists of the present invention, will also produce changes in hepatocyte proliferation, and epithelial cell proliferation in the lung, breast, pancreas, stomach, small intestine, and large intestine. Polynucleotides or polypeptides, as well as agonists or antagonists of the present invention, could promote proliferation of epithelial cells such as sebocytes, hair follicles, hepatocytes, type II pneumocytes, mucin-producing goblet cells, and other epithelial cells and their progenitors contained within the skin, lung, liver, and gastrointestinal tract. Polynucleotides or polypeptides, agonists or antagonists of the present invention, may promote proliferation of endothelial cells, keratinocytes, and basal keratinocytes.

Polynucleotides or polypeptides, as well as agonists or antagonists of the present invention, could also be used to reduce the side effects of gut toxicity that result from radiation, chemotherapy treatments or viral infections. Polynucleotides or polypeptides, as well as agonists or antagonists of the present invention, may have a cytoprotective effect on the small intestine mucosa. Polynucleotides or polypeptides, as well as agonists or antagonists of the present invention, may also stimulate healing of mucositis (mouth ulcers) that result from chemotherapy and viral infections.

Polynucleotides or polypeptides, as well as agonists or antagonists of the present invention, could further be used in full regeneration of skin in full and partial thickness skin defects, including burns, (i.e., repopulation of hair follicles, sweat glands, and sebaceous glands), treatment of other skin defects such as psoriasis. Polynucleotides or polypeptides, as well as agonists or antagonists of the present invention, could be used to treat epidermolysis bullosa, a defect in adherence of the epidermis to the underlying dermis which results in frequent, open and painful blisters by accelerating reepithelialization of these lesions. Polynucleotides or polypeptides, as well as agonists or antagonists of the present invention, could also be used to treat gastric and doudenal ulcers and help heal by scar formation of the mucosal lining and regeneration of glandular mucosa and duodenal mucosal lining more rapidly. Inflammatory bowel diseases, such as Crohn's disease and ulcerative colitis, are diseases which result in destruction of the mucosal surface of the small or large intestine, respectively. Thus, polynucleotides or polypeptides, as well as agonists or antagonists of the present invention, could be used to promote the resurfacing of the mucosal surface to aid more rapid healing and to prevent progression of inflammatory bowel disease. Treatment with polynucleotides or polypeptides, agonists or antagonists of the present invention, is expected to have a significant effect on the production of mucus throughout the gastrointestinal tract and could be used to protect the intestinal mucosa from injurious substances that are ingested or following surgery. Polynucleotides or polypeptides, as well as agonists or antagonists of the present invention, could be used to treat diseases associate with the under expression.

Moreover, polynucleotides or polypeptides, as well as agonists or antagonists of the present invention, could be used to prevent and heal damage to the lungs due to various pathological states. Polynucleotides or polypeptides, as well as agonists or antagonists of the present invention, which could stimulate proliferation and differentiation and promote the repair of alveoli and brochiolar epithelium to prevent or treat acute or chronic lung damage. For example, emphysema, which results in the progressive loss of aveoli, and inhalation injuries, i.e., resulting from smoke inhalation and burns, that cause necrosis of the bronchiolar epithelium and alveoli could be effectively treated using polynucleotides or polypeptides, agonists or antagonists of the present invention. Also, polynucleotides or polypeptides, as well as agonists or antagonists of the present invention, could be used to stimulate the proliferation of and differentiation of type II pneumocytes, which may help treat or prevent disease such as hyaline membrane diseases, such as infant respiratory distress syndrome and bronchopulmonary displasia, in premature infants.

Polynucleotides or polypeptides, as well as agonists or antagonists of the present invention, could stimulate the proliferation and differentiation of hepatocytes and, thus, could be used to alleviate or treat liver diseases and pathologies such as fulminant liver failure caused by cirrhosis, liver damage caused by viral hepatitis and toxic substances (i.e., acetaminophen, carbon tetraholoride and other hepatotoxins known in the art).

In addition, polynucleotides or polypeptides, as well as agonists or antagonists of the present invention, could be used treat or prevent the onset of diabetes mellitus. In patients with newly diagnosed Types I and II diabetes, where some islet cell function remains, polynucleotides or polypeptides, as well as agonists or antagonists of the present invention, could be used to maintain the islet function so as to alleviate, delay or prevent permanent manifestation of the disease. Also, polynucleotides or polypeptides, as well as agonists or antagonists of the present invention, could be used as an auxiliary in islet cell transplantation to improve or promote islet cell function.

Regeneration

Polynucleotides or polypeptides, as well as agonists or antagonists of the present invention can be used to differentiate, proliferate, and attract cells, leading to the regeneration of tissues. (See, Science 276:59-87 (1997)). The regeneration of tissues could be used to repair, replace, or protect tissue damaged by congenital defects, trauma (wounds, burns, incisions, or ulcers), age, disease (e.g. osteoporosis, osteocarthritis, periodontal disease, liver failure), surgery, including cosmetic plastic surgery, fibrosis, reperfusion injury, or systemic cytokine damage.

Tissues that could be regenerated using the present invention include organs (e.g., pancreas, liver, intestine, kidney, skin, endothelium), muscle (smooth, skeletal or cardiac), vasculature (including vascular and lymphatics), nervous, hematopoietic, and skeletal (bone, cartilage, tendon, and ligament) tissue. Preferably, regeneration occurs without or decreased scarring. Regeneration also may include angiogenesis.

Moreover, polynucleotides or polypeptides, as well as agonists or antagonists of the present invention, may increase regeneration of tissues difficult to heal. For example, increased tendon/ligament regeneration would quicken recovery time after damage. Polynucleotides or polypeptides, as well as agonists or antagonists of the present invention could also be used prophylactically in an effort to avoid damage. Specific diseases that could be treated include of tendinitis, carpal tunnel syndrome, and other tendon or ligament defects. A further example of tissue regeneration of non-healing wounds includes pressure ulcers, ulcers associated with vascular insufficiency, surgical, and traumatic wounds.

Similarly, nerve and brain tissue could also be regenerated by using polynucleotides or polypeptides, as well as agonists or antagonists of the present invention, to proliferate and differentiate nerve cells. Diseases that could be treated using this method include central and peripheral nervous system diseases, neuropathies, or mechanical and traumatic disorders (e.g., spinal cord disorders, head trauma, cerebrovascular disease, and stoke). Specifically, diseases associated with peripheral nerve injuries, peripheral neuropathy (e.g., resulting from chemotherapy or other medical therapies), localized neuropathies, and central nervous system diseases (e.g., Alzheimer's disease, Parkinson's disease, Huntington's disease, amyotrophic lateral sclerosis, and Shy-Drager syndrome), could all be treated using the polynucleotides or polypeptides, as well as agonists or antagonists of the present invention.

Chemotaxis

Polynucleotides or polypeptides, as well as agonists or antagonists of the present invention may have chemotaxis activity. A chemotaxic molecule attracts or mobilizes cells (e.g., monocytes, fibroblasts, neutrophils, T-cells, mast cells, eosinophils, epithelial and/or endothelial cells) to a particular site in the body, such as inflammation, infection, or site of hyperproliferation. The mobilized cells can then fight off and/or heal the particular trauma or abnormality.

Polynucleotides or polypeptides, as well as agonists or antagonists of the present invention may increase chemotaxic activity of particular cells. These chemotactic molecules can then be used to treat inflammation, infection, hyperproliferative disorders, or any immune system disorder by increasing the number of cells targeted to a particular location in the body. For example, chemotaxic molecules can be used to treat wounds and other trauma to tissues by attracting immune cells to the injured location. Chemotactic molecules of the present invention can also attract fibroblasts, which can be used to treat wounds.

It is also contemplated that polynucleotides or polypeptides, as well as agonists or antagonists of the present invention may inhibit chemotactic activity. These molecules could also be used to treat disorders. Thus, polynucleotides or polypeptides, as well as agonists or antagonists of the present invention could be used as an inhibitor of chemotaxis.

Binding Activity

A polypeptide of the present invention may be used to screen for molecules that bind to the polypeptide or for molecules to which the polypeptide binds. The binding of the polypeptide and the molecule may activate (agonist), increase, inhibit (antagonist), or decrease activity of the polypeptide or the molecule bound. Examples of such molecules include antibodies, oligonucleotides, proteins (e.g., receptors), or small molecules.

Preferably, the molecule is closely related to the natural ligand of the polypeptide, e.g., a fragment of the ligand, or a natural substrate, a ligand, a structural or functional mimetic. (See, Coligan et al., Current Protocols in Immunology 1(2):Chapter 5 (1991)). Similarly, the molecule can be closely related to the natural receptor to which the polypeptide binds, or at least, a fragment of the receptor capable of being bound by the polypeptide (e.g., active site). In either case, the molecule can be rationally designed using known techniques.

Preferably, the screening for these molecules involves producing appropriate cells which express the polypeptide. Preferred cells include cells from mammals, yeast, Drosophila, or E. coli. Cells expressing the polypeptide (or cell membrane containing the expressed polypeptide) are then preferably contacted with a test compound potentially containing the molecule to observe binding, stimulation, or inhibition of activity of either the polypeptide or the molecule.

The assay may simply test binding of a candidate compound to the polypeptide, wherein binding is detected by a label, or in an assay involving competition with a labeled competitor. Further, the assay may test whether the candidate compound results in a signal generated by binding to the polypeptide.

Alternatively, the assay can be carried out using cell-free preparations, polypeptide/molecule affixed to a solid support, chemical libraries, or natural product mixtures. The assay may also simply comprise the steps of mixing a candidate compound with a solution containing a polypeptide, measuring polypeptide/molecule activity or binding, and comparing the polypeptide/molecule activity or binding to a standard.

Preferably, an ELISA assay can measure polypeptide level or activity in a sample (e.g., biological sample) using a monoclonal or polyclonal antibody. The antibody can measure polypeptide level or activity by either binding, directly or indirectly, to the polypeptide or by competing with the polypeptide for a substrate.

Additionally, the receptor to which the polypeptide of the present invention binds can be identified by numerous methods known to those of skill in the art, for example, ligand panning and FACS sorting (Coligan, et al., Current Protocols in Immun., 1(2), Chapter 5, (1991)). For example, expression cloning is employed wherein polyadenylated RNA is prepared from a cell responsive to the polypeptides, for example, NIH3T3 cells which are known to contain multiple receptors for the FGF family proteins, and SC-3 cells, and a cDNA library created from this RNA is divided into pools and used to transfect COS cells or other cells that are not responsive to the polypeptides. Transfected cells which are grown on glass slides are exposed to the polypeptide of the present invention, after they have been labeled. The polypeptides can be labeled by a variety of means including iodination or inclusion of a recognition site for a site-specific protein kinase.

Following fixation and incubation, the slides are subjected to auto-radiographic analysis. Positive pools are identified and sub-pools are prepared and re-transfected using an iterative sub-pooling and re-screening process, eventually yielding a single clones that encodes the putative receptor.

As an alternative approach for receptor identification, the labeled polypeptides can be photoaffinity linked with cell membrane or extract preparations that express the receptor molecule. Cross-linked material is resolved by PAGE analysis and exposed to X-ray film. The labeled complex containing the receptors of the polypeptides can be excised, resolved into peptide fragments, and subjected to protein microsequencing. The amino acid sequence obtained from microsequencing would be used to design a set of degenerate oligonucleotide probes to screen a cDNA library to identify the genes encoding the putative receptors.

Moreover, the techniques of gene-shuffling, motif-shuffling, exon-shuffling, and/or codon-shuffling (collectively referred to as “DNA shuffling”) may be employed to modulate the activities of the polypeptide of the present invention thereby effectively generating agonists and antagonists of the polypeptide of the present invention. See generally, U.S. Pat. Nos. 5,605,793, 5,811,238, 5,830,721, 5,834,252, and 5,837,458, and Patten, P. A., et al., Curr. Opinion Biotechnol. 8:724-33 (1997); Harayama, S. Trends Biotechnol. 16(2):76-82 (1998); Hansson, L. O., et al., J. Mol. Biol. 287:265-76 (1999); and Lorenzo, M. M. and Blasco, R. Biotechniques 24(2):308-13 (1998); each of these patents and publications are hereby incorporated by reference). In one embodiment, alteration of polynucleotides and corresponding polypeptides may be achieved by DNA shuffling. DNA shuffling involves the assembly of two or more DNA segments into a desired molecule by homologous, or site-specific, recombination. In another embodiment, polynucleotides and corresponding polypeptides may be altered by being subjected to random mutagenesis by error-prone PCR, random nucleotide insertion or other methods prior to recombination. In another embodiment, one or more components, motifs, sections, parts, domains, fragments, etc., of the polypeptide of the present invention may be recombined with one or more components, motifs, sections, parts, domains, fragments, etc. of one or more heterologous molecules. In preferred embodiments, the heterologous molecules are family members. In further preferred embodiments, the heterologous molecule is a growth factor such as, for example, platelet-derived growth factor (PDGF), insulin-like growth factor (IGF-I), transforming growth factor (TGF)-alpha, epidermal growth factor (EGF), fibroblast growth factor (FGF), TGF-beta, bone morphogenetic protein (BMP)-2, BMP-4, BMP-5, BMP-6, BMP-7, activins A and B, decapentaplegic (dpp), 60A, OP-2, dorsalin, growth differentiation factors (GDFs), nodal, MIS, inhibin-alpha, TGF-beta1, TGF-beta2, TGF-beta3, TGF-beta5, and glial-derived neurotrophic factor (GDNF).

Other preferred fragments are biologically active fragments of the polypeptide of the present invention. Biologically active fragments are those exhibiting activity similar, but not necessarily identical, to an activity of the polypeptide of the present invention. The biological activity of the fragments may include an improved desired activity, or a decreased undesirable activity.

Additionally, this invention provides a method of screening compounds to identify those which modulate the action of the polypeptide of the present invention. An example of such an assay comprises combining a mammalian fibroblast cell, a the polypeptide of the present invention, the compound to be screened and ³[H]thymidine under cell culture conditions where the fibroblast cell would normally proliferate. A control assay may be performed in the absence of the compound to be screened and compared to the amount of fibroblast proliferation in the presence of the compound to determine if the compound stimulates proliferation by determining the uptake of ³[H] thymidine in each case. The amount of fibroblast cell proliferation is measured by liquid scintillation chromatography which measures the incorporation of ³[H] thymidine. Both agonist and antagonist compounds may be identified by this procedure.

In another method, a mammalian cell or membrane preparation expressing a receptor for a polypeptide of the present invention is incubated with a labeled polypeptide of the present invention in the presence of the compound. The ability of the compound to enhance or block this interaction could then be measured. Alternatively, the response of a known second messenger system following interaction of a compound to be screened and the receptor is measured and the ability of the compound to bind to the receptor and elicit a second messenger response is measured to determine if the compound is a potential agonist or antagonist. Such second messenger systems include but are not limited to, cAMP guanylate cyclase, ion channels or phosphoinositide hydrolysis.

All of these above assays can be used as diagnostic or prognostic markers. The molecules discovered using these assays can be used to treat disease or to bring about a particular result in a patient (e.g., blood vessel growth) by activating or inhibiting the polypeptide/molecule. Moreover, the assays can discover agents which may inhibit or enhance the production of the polypeptides of the invention from suitably manipulated cells or tissues.

Therefore, the invention includes a method of identifying compounds which bind to a polypeptide of the invention comprising the steps of: (a) incubating a candidate binding compound with a polypeptide of the present invention; and (b) determining if binding has occurred. Moreover, the invention includes a method of identifying agonists/antagonists comprising the steps of: (a) incubating a candidate compound with a polypeptide of the present invention, (b) assaying a biological activity, and (b) determining if a biological activity of the polypeptide has been altered.

Targeted Delivery

In another embodiment, the invention provides a method of delivering compositions to targeted cells expressing a receptor for a polypeptide of the invention, or cells expressing a cell bound form of a polypeptide of the invention.

As discussed herein, polypeptides or antibodies of the invention may be associated with heterologous polypeptides, heterologous nucleic acids, toxins, or prodrugs via hydrophobic, hydrophilic, ionic and/or covalent interactions. In one embodiment, the invention provides a method for the specific delivery of compositions of the invention to cells by administering polypeptides of the invention (including antibodies) that are associated with heterologous polypeptides or nucleic acids. In one example, the invention provides a method for delivering a therapeutic protein into the targeted cell. In another example, the invention provides a method for delivering a single stranded nucleic acid (e.g., antisense or ribozymes) or double stranded nucleic acid (e.g., DNA that can integrate into the cell's genome or replicate episomally and that can be transcribed) into the targeted cell.

In another embodiment, the invention provides a method for the specific destruction of cells (e.g., the destruction of tumor cells) by administering polypeptides of the invention (e.g., polypeptides of the invention or antibodies of the invention) in association with toxins or cytotoxic prodrugs.

By “toxin” is meant compounds that bind and activate endogenous cytotoxic effector systems, radioisotopes, holotoxins, modified toxins, catalytic subunits of toxins, or any molecules or enzymes not normally present in or on the surface of a cell that under defined conditions cause the cell's death. Toxins that may be used according to the methods of the invention include, but are not limited to, radioisotopes known in the art, compounds such as, for example, antibodies (or complement fixing containing portions thereof) that bind an inherent or induced endogenous cytotoxic effector system, thymidine kinase, endonuclease, RNAse, alpha toxin, ricin, abrin, Pseudomonas exotoxin A, diphtheria toxin, saporin, momordin, gelonin, pokeweed antiviral protein, alpha-sarcin and cholera toxin. By “cytotoxic prodrug” is meant a non-toxic compound that is converted by an enzyme, normally present in the cell, into a cytotoxic compound. Cytotoxic prodrugs that may be used according to the methods of the invention include, but are not limited to, glutamyl derivatives of benzoic acid mustard alkylating agent, phosphate derivatives of etoposide or mitomycin C, cytosine arabinoside, daunorubisin, and phenoxyacetamide derivatives of doxorubicin.

Drug Screening

Further contemplated is the use of the polypeptides of the present invention, or the polynucleotides encoding these polypeptides, to screen for molecules which modify the activities of the polypeptides of the present invention. Such a method would include contacting the polypeptide of the present invention with a selected compound(s) suspected of having antagonist or agonist activity, and assaying the activity of these polypeptides following binding.

This invention is particularly useful for screening therapeutic compounds by using the polypeptides of the present invention, or binding fragments thereof, in any of a variety of drug screening techniques. The polypeptide or fragment employed in such a test may be affixed to a solid support, expressed on a cell surface, free in solution, or located intracellularly. One method of drug screening utilizes eukaryotic or prokaryotic host cells which are stably transformed with recombinant nucleic acids expressing the polypeptide or fragment. Drugs are screened against such transformed cells in competitive binding assays. One may measure, for example, the formulation of complexes between the agent being tested and a polypeptide of the present invention.

Thus, the present invention provides methods of screening for drugs or any other agents which affect activities mediated by the polypeptides of the present invention. These methods comprise contacting such an agent with a polypeptide of the present invention or a fragment thereof and assaying for the presence of a complex between the agent and the polypeptide or a fragment thereof, by methods well known in the art. In such a competitive binding assay, the agents to screen are typically labeled. Following incubation, free agent is separated from that present in bound form, and the amount of free or uncomplexed label is a measure of the ability of a particular agent to bind to the polypeptides of the present invention.

Another technique for drug screening provides high throughput screening for compounds having suitable binding affinity to the polypeptides of the present invention, and is described in great detail in European Patent Application 84/03564, published on Sep. 13, 1984, which is incorporated herein by reference herein. Briefly stated, large numbers of different small peptide test compounds are synthesized on a solid substrate, such as plastic pins or some other surface. The peptide test compounds are reacted with polypeptides of the present invention and washed. Bound polypeptides are then detected by methods well known in the art. Purified polypeptides are coated directly onto plates for use in the aforementioned drug screening techniques. In addition, non-neutralizing antibodies may be used to capture the peptide and immobilize it on the solid support.

This invention also contemplates the use of competitive drug screening assays in which neutralizing antibodies capable of binding polypeptides of the present invention specifically compete with a test compound for binding to the polypeptides or fragments thereof. In this manner, the antibodies are used to detect the presence of any peptide which shares one or more antigenic epitopes with a polypeptide of the invention.

Antisense and Ribozyme (Antagonists)

In specific embodiments, antagonists according to the present invention are nucleic acids corresponding to the sequences contained in SEQ ID NO:X, or the complementary strand thereof, and/or to cDNA sequences contained in cDNA ATCC™ Deposit No:Z identified for example, in Table 1A and/or 1B. In one embodiment, antisense sequence is generated internally, by the organism, in another embodiment, the antisense sequence is separately administered (see, for example, O'Connor, J., Neurochem. 56:560 (1991). Oligodeoxynucleotides as Antisense Inhibitors of Gene Expression, CRC Press, Boca Raton, Fla. (1988). Antisense technology can be used to control gene expression through antisense DNA or RNA, or through triple-helix formation. Antisense techniques are discussed for example, in Okano, J., Neurochem. 56:560 (1991); Oligodeoxynucleotides as Antisense Inhibitors of Gene Expression, CRC Press, Boca Raton, Fla. (1988). Triple helix formation is discussed in, for instance, Lee et al., Nucleic Acids Research 6:3073 (1979); Cooney et al., Science 241:456 (1988); and Dervan et al., Science 251:1300 (1991). The methods are based on binding of a polynucleotide to a complementary DNA or RNA.

For example, the use of c-myc and c-myb antisense RNA constructs to inhibit the growth of the non-lymphocytic leukemia cell line HL-60 and other cell lines was previously described. (Wickstrom et al. (1988); Anfossi et al. (1989)). These experiments were performed in vitro by incubating cells with the oligoribonucleotide. A similar procedure for in vivo use is described in WO 91/15580. Briefly, a pair of oligonucleotides for a given antisense RNA is produced as follows: A sequence complimentary to the first 15 bases of the open reading frame is flanked by an EcoR1 site on the 5 end and a HindIII site on the 3 end. Next, the pair of oligonucleotides is heated at 90° C. for one minute and then annealed in 2× ligation buffer (20 mM TRIS HCl pH 7.5, 10 mM MgCl2, 10mM dithiothreitol (DTT) and 0.2 mM ATP) and then ligated to the EcoR1/Hind III site of the retroviral vector PMV7 (WO 91/15580).

For example, the 5′ coding portion of a polynucleotide that encodes the polypeptide of the present invention may be used to design an antisense RNA oligonucleotide of from about 10 to 40 base pairs in length. A DNA oligonucleotide is designed to be complementary to a region of the gene involved in transcription thereby preventing transcription and the production of the receptor. The antisense RNA oligonucleotide hybridizes to the mRNA in vivo and blocks translation of the mRNA molecule into receptor polypeptide.

In one embodiment, the antisense nucleic acid of the invention is produced intracellularly by transcription from an exogenous sequence. For example, a vector or a portion thereof, is transcribed, producing an antisense nucleic acid (RNA) of the invention. Such a vector would contain a sequence encoding the antisense nucleic acid. Such a vector can remain episomal or become chromosomally integrated, as long as it can be transcribed to produce the desired antisense RNA. Such vectors can be constructed by recombinant DNA technology methods standard in the art. Vectors can be plasmid, viral, or others known in the art, used for replication and expression in vertebrate cells. Expression of the sequence encoding the polypeptide of the present invention or fragments thereof, can be by any promoter known in the art to act in vertebrate, preferably human cells. Such promoters can be inducible or constitutive. Such promoters include, but are not limited to, the SV40 early promoter region (Bernoist and Chambon, Nature 29:304-310 (1981), the promoter contained in the 3′ long terminal repeat of Rous sarcoma virus (Yamamoto et al., Cell 22:787-797 (1980), the herpes thymidine promoter (Wagner et al., Proc. Natl. Acad. Sci. U.S.A. 78:1441-1445 (1981), the regulatory sequences of the metallothionein gene (Brinster, et al., Nature 296:39-42 (1982)), etc.

The antisense nucleic acids of the invention comprise a sequence complementary to at least a portion of an RNA transcript of a gene of the present invention. However, absolute complementarity, although preferred, is not required. A sequence “complementary to at least a portion of an RNA,” referred to herein, means a sequence having sufficient complementarity to be able to hybridize with the RNA, forming a stable duplex; in the case of double stranded antisense nucleic acids, a single strand of the duplex DNA may thus be tested, or triplex formation may be assayed. The ability to hybridize will depend on both the degree of complementarity and the length of the antisense nucleic acid. Generally, the larger the hybridizing nucleic acid, the more base mismatches with a RNA it may contain and still form a stable duplex (or triplex as the case may be). One skilled in the art can ascertain a tolerable degree of mismatch by use of standard procedures to determine the melting point of the hybridized complex.

Oligonucleotides that are complementary to the 5′ end of the message, e.g., the 5′ untranslated sequence up to and including the AUG initiation codon, should work most efficiently at inhibiting translation. However, sequences complementary to the 3′ untranslated sequences of mRNAs have been shown to be effective at inhibiting translation of mRNAs as well. See generally, Wagner, R., 1994, Nature 372:333-335. Thus, oligonucleotides complementary to either the 5′- or 3′-non-translated, non-coding regions of polynucleotide sequences described herein could be used in an antisense approach to inhibit translation of endogenous mRNA. Oligonucleotides complementary to the 5′ untranslated region of the mRNA should include the complement of the AUG start codon. Antisense oligonucleotides complementary to mRNA coding regions are less efficient inhibitors of translation but could be used in accordance with the invention. Whether designed to hybridize to the 5′-, 3′- or coding region of mRNA of the present invention, antisense nucleic acids should be at least six nucleotides in length, and are preferably oligonucleotides ranging from 6 to about 50 nucleotides in length. In specific aspects the oligonucleotide is at least 10 nucleotides, at least 17 nucleotides, at least 25 nucleotides or at least 50 nucleotides.

The polynucleotides of the invention can be DNA or RNA or chimeric mixtures or derivatives or modified versions thereof, single-stranded or double-stranded. The oligonucleotide can be modified at the base moiety, sugar moiety, or phosphate backbone, for example, to improve stability of the molecule, hybridization, etc. The oligonucleotide may include other appended groups such as peptides (e.g., for targeting host cell receptors in vivo), or agents facilitating transport across the cell membrane (see, e.g., Letsinger et al., 1989, Proc. Natl. Acad. Sci. U.S.A. 86:6553-6556; Lemaitre et al., 1987, Proc. Natl. Acad. Sci. 84:648-652; PCT Publication No. WO88/09810, published Dec. 15, 1988) or the blood-brain barrier (see, e.g., PCT Publication No. WO89/10134, published Apr. 25, 1988), hybridization-triggered cleavage agents. (See, e.g., Krol et al., 1988, BioTechniques 6:958-976) or intercalating agents. (See, e.g., Zon, 1988, Pharm. Res. 5:539-549). To this end, the oligonucleotide may be conjugated to another molecule, e.g., a peptide, hybridization triggered cross-linking agent, transport agent, hybridization-triggered cleavage agent, etc.

The antisense oligonucleotide may comprise at least one modified base moiety which is selected from the group including, but not limited to, 5-fluorouracil, 5-bromouracil, 5-chlorouracil, 5-iodouracil, hypoxanthine, xantine, 4-acetylcytosine, 5-(carboxyhydroxylmethyl) uracil, 5-carboxymethylaminomethyl-2-thiouridine, 5-carboxymethylaminomethyluracil, dihydrouracil, beta-D-galactosylqueosine, inosine, N6-isopentenyladenine, 1-methylguanine, 1-methylinosine, 2,2-dimethylguanine, 2-methyladenine, 2-methylguanine, 3-methylcytosine, 5-methylcytosine, N6-adenine, 7-methylguanine, 5-methylaminomethyluracil, 5-methoxyaminomethyl-2-thiouracil, beta-D-mannosylqueosine, 5′-methoxycarboxymethyluracil, 5-methoxyuracil, 2-methylthio-N6-isopentenyladenine, uracil-5-oxyacetic acid (v), wybutoxosine, pseudouracil, queosine, 2-thiocytosine, 5-methyl-2-thiouracil, 2-thiouracil, 4-thiouracil, 5-methyluracil, uracil-5-oxyacetic acid methylester, uracil-5-oxyacetic acid (v), 5-methyl-2-thiouracil, 3-(3-amino-3-N-2-carboxypropyl)uracil, (acp3)w, and 2,6-diaminopurine.

The antisense oligonucleotide may also comprise at least one modified sugar moiety selected from the group including, but not limited to, arabinose, 2-fluoroarabinose, xylulose, and hexose.

In yet another embodiment, the antisense oligonucleotide comprises at least one modified phosphate backbone selected from the group including, but not limited to, a phosphorothioate, a phosphorodithioate, a phosphoramidothioate, a phosphoramidate, a phosphordiamidate, a methylphosphonate, an alkyl phosphotriester, and a formacetal or analog thereof.

In yet another embodiment, the antisense oligonucleotide is an a-anomeric oligonucleotide. An a-anomeric oligonucleotide forms specific double-stranded hybrids with complementary RNA in which, contrary to the usual b-units, the strands run parallel to each other (Gautier et al., 1987, Nucl. Acids Res. 15:6625-6641). The oligonucleotide is a 2′-0-methylribonucleotide (Inoue et al., 1987, Nucl. Acids Res. 15:6131-6148), or a chimeric RNA-DNA analogue (Inoue et al., 1987, FEBS Lett. 215:327-330).

Polynucleotides of the invention may be synthesized by standard methods known in the art, e.g. by use of an automated DNA synthesizer (such as are commercially available from Biosearch, Applied Biosystems, etc.). As examples, phosphorothioate oligonucleotides may be synthesized by the method of Stein et al. (1988, Nucl. Acids Res. 16:3209), methylphosphonate oligonucleotides can be prepared by use of controlled pore glass polymer supports (Sarin et al., 1988, Proc. Natl. Acad. Sci. U.S.A. 85:7448-7451), etc.

While antisense nucleotides complementary to the coding region sequence could be used, those complementary to the transcribed untranslated region are most preferred.

Potential antagonists according to the invention also include catalytic RNA, or a ribozyme (See, e.g., PCT International Publication WO 90/11364, published Oct. 4, 1990; Sarver et al., Science 247:1222-1225 (1990). While ribozymes that cleave mRNA at site specific recognition sequences can be used to destroy mRNAs, the use of hammerhead ribozymes is preferred. Hammerhead ribozymes cleave mRNAs at locations dictated by flanking regions that form complementary base pairs with the target mRNA. The sole requirement is that the target mRNA have the following sequence of two bases: 5′-UG-3′. The construction and production of hammerhead ribozymes is well known in the art and is described more fully in Haseloff and Gerlach, Nature 334:585-591 (1988). There are numerous potential hammerhead ribozyme cleavage sites within the nucleotide sequence of SEQ ID NO:X. Preferably, the ribozyme is engineered so that the cleavage recognition site is located near the 5′ end of the mRNA; i.e., to increase efficiency and minimize the intracellular accumulation of non-functional mRNA transcripts.

As in the antisense approach, the ribozymes of the invention can be composed of modified oligonucleotides (e.g., for improved stability, targeting, etc.) and should be delivered to cells which express in vivo. DNA constructs encoding the ribozyme may be introduced into the cell in the same manner as described above for the introduction of antisense encoding DNA. A preferred method of delivery involves using a DNA construct “encoding” the ribozyme under the control of a strong constitutive promoter, such as, for example, pol III or pol II promoter, so that transfected cells will produce sufficient quantities of the ribozyme to destroy endogenous messages and inhibit translation. Since ribozymes unlike antisense molecules, are catalytic, a lower intracellular concentration is required for efficiency.

Antagonist/agonist compounds may be employed to inhibit the cell growth and proliferation effects of the polypeptides of the present invention on neoplastic cells and tissues, i.e. stimulation of angiogenesis of tumors, and, therefore, retard or prevent abnormal cellular growth and proliferation, for example, in tumor formation or growth.

The antagonist/agonist may also be employed to prevent hyper-vascular diseases, and prevent the proliferation of epithelial lens cells after extracapsular cataract surgery. Prevention of the mitogenic activity of the polypeptides of the present invention may also be desirous in cases such as restenosis after balloon angioplasty.

The antagonist/agonist may also be employed to prevent the growth of scar tissue during wound healing.

The antagonist/agonist may also be employed to treat the diseases described herein.

Thus, the invention provides a method of treating disorders or diseases, including but not limited to the disorders or diseases listed throughout this application, associated with overexpression of a polynucleotide of the present invention by administering to a patient (a) an antisense molecule directed to the polynucleotide of the present invention, and/or (b) a ribozyme directed to the polynucleotide of the present invention.

Binding Peptides and Other Molecules

The invention also encompasses screening methods for identifying polypeptides and nonpolypeptides that bind polypeptides of the invention, and the binding molecules identified thereby. These binding molecules are useful, for example, as agonists and antagonists of the polypeptides of the invention. Such agonists and antagonists can be used, in accordance with the invention, in the therapeutic embodiments described in detail, below.

This method comprises the steps of:

contacting polypeptides of the invention with a plurality of molecules; and

identifying a molecule that binds the polypeptides of the invention.

The step of contacting the polypeptides of the invention with the plurality of molecules may be effected in a number of ways. For example, one may contemplate immobilizing the polypeptides on a solid support and bringing a solution of the plurality of molecules in contact with the immobilized polypeptides. Such a procedure would be akin to an affinity chromatographic process, with the affinity matrix being comprised of the immobilized polypeptides of the invention. The molecules having a selective affinity for the polypeptides can then be purified by affinity selection. The nature of the solid support, process for attachment of the polypeptides to the solid support, solvent, and conditions of the affinity isolation or selection are largely conventional and well known to those of ordinary skill in the art.

Alternatively, one may also separate a plurality of polypeptides into substantially separate fractions comprising a subset of or individual polypeptides. For instance, one can separate the plurality of polypeptides by gel electrophoresis, column chromatography, or like method known to those of ordinary skill for the separation of polypeptides. The individual polypeptides can also be produced by a transformed host cell in such a way as to be expressed on or about its outer surface (e.g., a recombinant phage). Individual isolates can then be “probed” by the polypeptides of the invention, optionally in the presence of an inducer should one be required for expression, to determine if any selective affinity interaction takes place between the polypeptides and the individual clone. Prior to contacting the polypeptides with each fraction comprising individual polypeptides, the polypeptides could first be transferred to a solid support for additional convenience. Such a solid support may simply be a piece of filter membrane, such as one made of nitrocellulose or nylon. In this manner, positive clones could be identified from a collection of transformed host cells of an expression library, which harbor a DNA construct encoding a polypeptide having a selective affinity for polypeptides of the invention. Furthermore, the amino acid sequence of the polypeptide having a selective affinity for the polypeptides of the invention can be determined directly by conventional means or the coding sequence of the DNA encoding the polypeptide can frequently be determined more conveniently. The primary sequence can then be deduced from the corresponding DNA sequence. If the amino acid sequence is to be determined from the polypeptide itself, one may use microsequencing techniques. The sequencing technique may include mass spectroscopy.

In certain situations, it may be desirable to wash away any unbound polypeptides from a mixture of the polypeptides of the invention and the plurality of polypeptides prior to attempting to determine or to detect the presence of a selective affinity interaction. Such a wash step may be particularly desirable when the polypeptides of the invention or the plurality of polypeptides are bound to a solid support.

The plurality of molecules provided according to this method may be provided by way of diversity libraries, such as random or combinatorial peptide or nonpeptide libraries which can be screened for molecules that specifically bind polypeptides of the invention. Many libraries are known in the art that can be used, e.g., chemically synthesized libraries, recombinant (e.g., phage display libraries), and in vitro translation-based libraries. Examples of chemically synthesized libraries are described in Fodor et al., 1991, Science 251:767-773; Houghten et al., 1991, Nature 354:84-86; Lam et al., 1991, Nature 354:82-84; Medynski, 1994, Bio/Technology 12:709-710;Gallop et al., 1994, J. Medicinal Chemistry 37(9):1233-1251; Ohlmeyer et al., 1993, Proc. Natl. Acad. Sci. USA 90:10922-10926; Erb et al., 1994, Proc. Natl. Acad. Sci. USA 91:11422-11426; Houghten et al., 1992, Biotechniques 13:412; Jayawickreme et al., 1994, Proc. Natl. Acad. Sci. USA 91:1614-1618; Salmon et al., 1993, Proc. Natl. Acad. Sci. USA 90:11708-11712; PCT Publication No. WO 93/20242; and Brenner and Lerner, 1992, Proc. Natl. Acad. Sci. USA 89:5381-5383.

Examples of phage display libraries are described in Scott and Smith, 1990, Science 249:386-390; Devlin et al., 1990, Science, 249:404-406; Christian, R. B., et al., 1992, J. Mol. Biol. 227:711-718); Lenstra, 1992, J. Immunol. Meth. 152:149-157; Kay et al., 1993, Gene 128:59-65; and PCT Publication No. WO 94/18318 dated Aug. 18, 1994.

In vitro translation-based libraries include but are not limited to those described in PCT Publication No. WO 91/05058 dated Apr. 18, 1991; and Mattheakis et al., 1994, Proc. Natl. Acad. Sci. USA 91:9022-9026.

By way of examples of nonpeptide libraries, a benzodiazepine library (see e.g., Bunin et al., 1994, Proc. Natl. Acad. Sci. USA 91:4708-4712) can be adapted for use. Peptoid libraries (Simon et al., 1992, Proc. Natl. Acad. Sci. USA 89:9367-9371) can also be used. Another example of a library that can be used, in which the amide functionalities in peptides have been permethylated to generate a chemically transformed combinatorial library, is described by Ostresh et al. (1994, Proc. Natl. Acad. Sci. USA 91:11138-11142).

The variety of non-peptide libraries that are useful in the present invention is great. For example, Ecker and Crooke, 1995, Bio/Technology 13:351-360 list benzodiazepines, hydantoins, piperazinediones, biphenyls, sugar analogs, beta-mercaptoketones, arylacetic acids, acylpiperidines, benzopyrans, cubanes, xanthines, aminimides, and oxazolones as among the chemical species that form the basis of various libraries.

Non-peptide libraries can be classified broadly into two types: decorated monomers and oligomers. Decorated monomer libraries employ a relatively simple scaffold structure upon which a variety functional groups is added. Often the scaffold will be a molecule with a known useful pharmacological activity. For example, the scaffold might be the benzodiazepine structure.

Non-peptide oligomer libraries utilize a large number of monomers that are assembled together in ways that create new shapes that depend on the order of the monomers. Among the monomer units that have been used are carbamates, pyrrolinones, and morpholinos. Peptoids, peptide-like oligomers in which the side chain is attached to the alpha amino group rather than the alpha carbon, form the basis of another version of non-peptide oligomer libraries. The first non-peptide oligomer libraries utilized a single type of monomer and thus contained a repeating backbone. Recent libraries have utilized more than one monomer, giving the libraries added flexibility.

Screening the libraries can be accomplished by any of a variety of commonly known methods. See, e.g., the following references, which disclose screening of peptide libraries: Parmley and Smith, 1989, Adv. Exp. Med. Biol. 251:215-218; Scott and Smith, 1990, Science 249:386-390; Fowlkes et al., 1992; BioTechniques 13:422-427; Oldenburg et al., 1992, Proc. Natl. Acad. Sci. USA 89:5393-5397; Yu et al., 1994, Cell 76:933-945; Staudt et al., 1988, Science 241:577-580; Bock et al., 1992, Nature 355:564-566; Tuerk et al., 1992, Proc. Natl. Acad. Sci. USA 89:6988-6992; Ellington et al., 1992, Nature 355:850-852; U.S. Pat. No. 5,096,815, U.S. Pat. No. 5,223,409, and U.S. Pat. No. 5,198,346, all to Ladner et al.; Rebar and Pabo, 1993, Science 263:671-673; and CT Publication No. WO 94/18318.

In a specific embodiment, screening to identify a molecule that binds polypeptides of the invention can be carried out by contacting the library members with polypeptides of the invention immobilized on a solid phase and harvesting those library members that bind to the polypeptides of the invention. Examples of such screening methods, termed “panning” techniques are described by way of example in Parmley and Smith, 1988, Gene 73:305-318; Fowlkes et al., 1992, BioTechniques 13:422-427; PCT Publication No. WO 94/18318; and in references cited herein.

In another embodiment, the two-hybrid system for selecting interacting proteins in yeast (Fields and Song, 1989, Nature 340:245-246; Chien et al., 1991, Proc. Natl. Acad. Sci. USA 88:9578-9582) can be used to identify molecules that specifically bind to polypeptides of the invention.

Where the binding molecule is a polypeptide, the polypeptide can be conveniently selected from any peptide library, including random peptide libraries, combinatorial peptide libraries, or biased peptide libraries. The term “biased” is used herein to mean that the method of generating the library is manipulated so as to restrict one or more parameters that govern the diversity of the resulting collection of molecules, in this case peptides.

Thus, a truly random peptide library would generate a collection of peptides in which the probability of finding a particular amino acid at a given position of the peptide is the same for all 20 amino acids. A bias can be introduced into the library, however, by specifying, for example, that a lysine occur every fifth amino acid or that positions 4, 8, and 9 of a decapeptide library be fixed to include only arginine. Clearly, many types of biases can be contemplated, and the present invention is not restricted to any particular bias. Furthermore, the present invention contemplates specific types of peptide libraries, such as phage displayed peptide libraries and those that utilize a DNA construct comprising a lambda phage vector with a DNA insert.

As mentioned above, in the case of a binding molecule that is a polypeptide, the polypeptide may have about 6 to less than about 60 amino acid residues, preferably about 6 to about 10 amino acid residues, and most preferably, about 6 to about 22 amino acids. In another embodiment, a binding polypeptide has in the range of 15-100 amino acids, or 20-50 amino acids.

The selected binding polypeptide can be obtained by chemical synthesis or recombinant expression.

Other Activities

A polypeptide, polynucleotide, agonist, or antagonist of the present invention, as a result of the ability to stimulate vascular endothelial cell growth, may be employed in treatment for stimulating re-vascularization of ischemic tissues due to various disease conditions such as thrombosis, arteriosclerosis, and other cardiovascular conditions. The polypeptide, polynucleotide, agonist, or antagonist of the present invention may also be employed to stimulate angiogenesis and limb regeneration, as discussed above.

A polypeptide, polynucleotide, agonist, or antagonist of the present invention may also be employed for treating wounds due to injuries, burns, post-operative tissue repair, and ulcers since they are mitogenic to various cells of different origins, such as fibroblast cells and skeletal muscle cells, and therefore, facilitate the repair or replacement of damaged or diseased tissue.

A polypeptide, polynucleotide, agonist, or antagonist of the present invention may also be employed stimulate neuronal growth and to treat and prevent neuronal damage which occurs in certain neuronal disorders or neuro-degenerative conditions such as Alzheimer's disease, Parkinson's disease, and AIDS-related complex. A polypeptide, polynucleotide, agonist, or antagonist of the present invention may have the ability to stimulate chondrocyte growth, therefore, they may be employed to enhance bone and periodontal regeneration and aid in tissue transplants or bone grafts.

A polypeptide, polynucleotide, agonist, or antagonist of the present invention may be also be employed to prevent skin aging due to sunburn by stimulating keratinocyte growth.

A polypeptide, polynucleotide, agonist, or antagonist of the present invention may also be employed for preventing hair loss, since FGF family members activate hair-forming cells and promotes melanocyte growth. Along the same lines, a polypeptide, polynucleotide, agonist, or antagonist of the present invention may be employed to stimulate growth and differentiation of hematopoietic cells and bone marrow cells when used in combination with other cytokines.

A polypeptide, polynucleotide, agonist, or antagonist of the present invention may also be employed to maintain organs before transplantation or for supporting cell culture of primary tissues. A polypeptide, polynucleotide, agonist, or antagonist of the present invention may also be employed for inducing tissue of mesodermal origin to differentiate in early embryos.

A polypeptide, polynucleotide, agonist, or antagonist of the present invention may also increase or decrease the differentiation or proliferation of embryonic stem cells, besides, as discussed above, hematopoietic lineage.

A polypeptide, polynucleotide, agonist, or antagonist of the present invention may also be used to modulate mammalian characteristics, such as body height, weight, hair color, eye color, skin, percentage of adipose tissue, pigmentation, size, and shape (e.g., cosmetic surgery). Similarly, a polypeptide, polynucleotide, agonist, or antagonist of the present invention may be used to modulate mammalian metabolism affecting catabolism, anabolism, processing, utilization, and storage of energy.

A polypeptide, polynucleotide, agonist, or antagonist of the present invention may be used to change a mammal's mental state or physical state by influencing biorhythms, caricadic rhythms, depression (including depressive disorders), tendency for violence, tolerance for pain, reproductive capabilities (preferably by Activin or Inhibin-like activity), hormonal or endocrine levels, appetite, libido, memory, stress, or other cognitive qualities.

A polypeptide, polynucleotide, agonist, or antagonist of the present invention may also be used as a food additive or preservative, such as to increase or decrease storage capabilities, fat content, lipid, protein, carbohydrate, vitamins, minerals, cofactors or other nutritional components.

The above-recited applications have uses in a wide variety of hosts. Such hosts include, but are not limited to, human, murine, rabbit, goat, guinea pig, camel, horse, mouse, rat, hamster, pig, micro-pig, chicken, goat, cow, sheep, dog, cat, non-human primate, and human. In specific embodiments, the host is a mouse, rabbit, goat, guinea pig, chicken, rat, hamster, pig, sheep, dog or cat. In preferred embodiments, the host is a mammal. In most preferred embodiments, the host is a human.

OTHER PREFERRED EMBODIMENTS

Other preferred embodiments of the claimed invention include an isolated nucleic acid molecule comprising a nucleotide sequence which is at least 95% identical to a sequence of at least about 50 contiguous nucleotides in the nucleotide sequence of SEQ ID NO:X or the complementary strand thereto, the nucleotide sequence as defined in Table 1B or columns 8 and 9 of Table 2 or the complementary strand thereto, and/or cDNA contained in ATCC™ Deposit No:Z.

Also preferred is a nucleic acid molecule wherein said sequence of contiguous nucleotides is included in the nucleotide sequence of the portion of SEQ ID NO:X as defined in column 5, “ORF (From-To)”, in Table 1B.1.

Also preferred is a nucleic acid molecule wherein said sequence of contiguous nucleotides is included in the nucleotide sequence of the portion of SEQ ID NO:X as defined in columns 8 and 9, “NT From” and “NT To” respectively, in Table 2.

Also preferred is an isolated nucleic acid molecule comprising a nucleotide sequence which is at least 95% identical to a sequence of at least about 150 contiguous nucleotides in the nucleotide sequence of SEQ ID NO:X or the complementary strand thereto, the nucleotide sequence as defined in Table 1B or columns 8 and 9 of Table 2 or the complementary strand thereto, and/or cDNA contained in ATCC™ Deposit No:Z.

Further preferred is an isolated nucleic acid molecule comprising a nucleotide sequence which is at least 95% identical to a sequence of at least about 500 contiguous nucleotides in the nucleotide sequence of SEQ ID NO:X or the complementary strand thereto, the nucleotide sequence as defined in Table 1B or columns 8 and 9 of Table 2 or the complementary strand thereto, and/or cDNA contained in ATCC™ Deposit No:Z.

A further preferred embodiment is a nucleic acid molecule comprising a nucleotide sequence which is at least 95% identical to the nucleotide sequence of the portion of SEQ ID NO:X defined in column 5, “ORF (From-To)”, in Table 1B.1.

A further preferred embodiment is a nucleic acid molecule comprising a nucleotide sequence which is at least 95% identical to the nucleotide sequence of the portion of SEQ ID NO:X defined in columns 8 and 9, “NT From” and “NT To”, respectively, in Table 2.

A further preferred embodiment is an isolated nucleic acid molecule comprising a nucleotide sequence which is at least 95% identical to the complete nucleotide sequence of SEQ ID NO:X or the complementary strand thereto, the nucleotide sequence as defined in column 5 of Table 1B.1 or columns 8 and 9 of Table 2 or the complementary strand thereto, and/or cDNA contained in ATCC™ Deposit No:Z.

Also preferred is an isolated nucleic acid molecule which hybridizes under stringent hybridization conditions to a nucleic acid molecule comprising a nucleotide sequence of SEQ ID NO:X or the complementary strand thereto, the nucleotide sequence as defined in column 5 of Table 1B.1 or columns 8 and 9 of Table 2 or the complementary strand thereto, and/or cDNA contained in ATCC™ Deposit No:Z, wherein said nucleic acid molecule which hybridizes does not hybridize under stringent hybridization conditions to a nucleic acid molecule having a nucleotide sequence consisting of only A residues or of only T residues.

Also preferred is a composition of matter comprising a DNA molecule which comprises the cDNA contained in ATCC™ Deposit No:Z.

Also preferred is an isolated nucleic acid molecule comprising a nucleotide sequence which is at least 95% identical to a sequence of at least 50 contiguous nucleotides of the cDNA sequence contained in ATCC™ Deposit No:Z.

Also preferred is an isolated nucleic acid molecule, wherein said sequence of at least 50 contiguous nucleotides is included in the nucleotide sequence of an open reading frame sequence encoded by cDNA contained in ATCC™ Deposit No:Z.

Also preferred is an isolated nucleic acid molecule comprising a nucleotide sequence which is at least 95% identical to sequence of at least 150 contiguous nucleotides in the nucleotide sequence encoded by cDNA contained in ATCC™ Deposit No:Z.

A further preferred embodiment is an isolated nucleic acid molecule comprising a nucleotide sequence which is at least 95% identical to sequence of at least 500 contiguous nucleotides in the nucleotide sequence encoded by cDNA contained in ATCC™ Deposit No:Z.

A further preferred embodiment is an isolated nucleic acid molecule comprising a nucleotide sequence which is at least 95% identical to the complete nucleotide sequence encoded by cDNA contained in ATCC™ Deposit No:Z.

A further preferred embodiment is a method for detecting in a biological sample a nucleic acid molecule comprising a nucleotide sequence which is at least 95% identical to a sequence of at least 50 contiguous nucleotides in a sequence selected from the group consisting of: a nucleotide sequence of SEQ ID NO:X or the complementary strand thereto; the nucleotide sequence as defined in column 5 of Table 1B.1 or columns 8 and 9 of Table 2 or the complementary strand thereto; and a nucleotide sequence encoded by cDNA contained in ATCC™ Deposit No:Z; which method comprises a step of comparing a nucleotide sequence of at least one nucleic acid molecule in said sample with a sequence selected from said group and determining whether the sequence of said nucleic acid molecule in said sample is at least 95% identical to said selected sequence.

Also preferred is the above method wherein said step of comparing sequences comprises determining the extent of nucleic acid hybridization between nucleic acid molecules in said sample and a nucleic acid molecule comprising said sequence selected from said group. Similarly, also preferred is the above method wherein said step of comparing sequences is performed by comparing the nucleotide sequence determined from a nucleic acid molecule in said sample with said sequence selected from said group. The nucleic acid molecules can comprise DNA molecules or RNA molecules.

A further preferred embodiment is a method for identifying the species, tissue or cell type of a biological sample which method comprises a step of detecting nucleic acid molecules in said sample, if any, comprising a nucleotide sequence that is at least 95% identical to a sequence of at least 50 contiguous nucleotides in a sequence selected from the group consisting of: a nucleotide sequence of SEQ ID NO:X or the complementary strand thereto; the nucleotide sequence as defined in column 5 of Table 1B.1 or columns 8 and 9 of Table 2 or the complementary strand thereto; and a nucleotide sequence of the cDNA contained in ATCC™ Deposit No:Z.

The method for identifying the species, tissue or cell type of a biological sample can comprise a step of detecting nucleic acid molecules comprising a nucleotide sequence in a panel of at least two nucleotide sequences, wherein at least one sequence in said panel is at least 95% identical to a sequence of at least 50 contiguous nucleotides in a sequence selected from said group.

Also preferred is a method for diagnosing in a subject a pathological condition associated with abnormal structure or expression of a nucleotide sequence of SEQ ID NO:X or the complementary strand thereto; the nucleotide sequence as defined in column 5 of Table 1B.1 or columns 8 and 9 of Table 2 or the complementary strand thereto; or the cDNA contained in ATCC™ Deposit No:Z which encodes a protein, wherein the method comprises a step of detecting in a biological sample obtained from said subject nucleic acid molecules, if any, comprising a nucleotide sequence that is at least 95% identical to a sequence of at least 50 contiguous nucleotides in a sequence selected from the group consisting of: a nucleotide sequence of SEQ ID NO:X or the complementary strand thereto; the nucleotide sequence as defined in column 5 of Table 1B.1 or columns 8 and 9 of Table 2 or the complementary strand thereto; and a nucleotide sequence of cDNA contained in ATCC™ Deposit No:Z.

The method for diagnosing a pathological condition can comprise a step of detecting nucleic acid molecules comprising a nucleotide sequence in a panel of at least two nucleotide sequences, wherein at least one sequence in said panel is at least 95% identical to a sequence of at least 50 contiguous nucleotides in a sequence selected from said group.

Also preferred is a composition of matter comprising isolated nucleic acid molecules wherein the nucleotide sequences of said nucleic acid molecules comprise a panel of at least two nucleotide sequences, wherein at least one sequence in said panel is at least 95% identical to a sequence of at least 50 contiguous nucleotides in a sequence selected from the group consisting of: a nucleotide sequence of SEQ ID NO:X or the complementary strand thereto; the nucleotide sequence as defined in column 5 of Table 1B.1 or columns 8 and 9 of Table 2 or the complementary strand thereto; and a nucleotide sequence encoded by cDNA contained in ATCC™ Deposit No:Z. The nucleic acid molecules can comprise DNA molecules or RNA molecules.

Also preferred is a composition of matter comprising isolated nucleic acid molecules wherein the nucleotide sequences of said nucleic acid molecules comprise a DNA microarray or “chip” of at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 15, 20, 25, 30, 40, 50, 100, 150, 200, 250, 300, 500, 1000, 2000, 3000, or 4000 nucleotide sequences, wherein at least one sequence in said DNA microarray or “chip” is at least 95% identical to a sequence of at least 50 contiguous nucleotides in a sequence selected from the group consisting of: a nucleotide sequence of SEQ ID NO:X wherein X is any integer as defined in Table 1A and/or 1B; and a nucleotide sequence encoded by a human cDNA clone identified by a cDNA “Clone ID” in Table 1A and/or 1B.

Also preferred is an isolated polypeptide comprising an amino acid sequence at least 90% identical to a sequence of at least about 10 contiguous amino acids in the polypeptide sequence of SEQ ID NO:Y; a polypeptide encoded by SEQ ID NO:X or the complementary strand thereto; the polypeptide encoded by the nucleotide sequence as defined in columns 8 and 9 of Table 2; and/or a polypeptide encoded by cDNA contained in ATCC™ Deposit No:Z.

Also preferred is an isolated polypeptide comprising an amino acid sequence at least 95% identical to a sequence of at least about 30 contiguous amino acids in the amino acid sequence of SEQ ID NO:Y; a polypeptide encoded by SEQ ID NO:X or the complementary strand thereto; the polypeptide encoded by the nucleotide sequence as defined in columns 8 and 9 of Table 2; and/or a polypeptide encoded by cDNA contained in ATCC™ Deposit No:Z.

Further preferred is an isolated polypeptide comprising an amino acid sequence at least 95% identical to a sequence of at least about 100 contiguous amino acids in the amino acid sequence of SEQ ID NO:Y; a polypeptide encoded by SEQ ID NO:X or the complementary strand thereto; the polypeptide encoded by the nucleotide sequence as defined in columns 8 and 9 of Table 2; and/or a polypeptide encoded by cDNA contained in ATCC™ Deposit No:Z.

Further preferred is an isolated polypeptide comprising an amino acid sequence at least 95% identical to the complete amino acid sequence of SEQ ID NO:Y; a polypeptide encoded by SEQ ID NO:X or the complementary strand thereto; the polypeptide encoded by the nucleotide sequence as defined in columns 8 and 9 of Table 2; and/or a polypeptide encoded by cDNA contained in ATCC™ Deposit No:Z.

Further preferred is an isolated polypeptide comprising an amino acid sequence at least 90% identical to a sequence of at least about 10 contiguous amino acids in the complete amino acid sequence of a polypeptide encoded by contained in ATCC™ Deposit No:Z Also preferred is a polypeptide wherein said sequence of contiguous amino acids is included in the amino acid sequence of a portion of said polypeptide encoded by cDNA contained in ATCC™ Deposit No:Z; a polypeptide encoded by SEQ ID NO:X or the complementary strand thereto; the polypeptide encoded by the nucleotide sequence as defined in columns 8 and 9 of Table 2; and/or the polypeptide sequence of SEQ ID NO:Y.

Also preferred is an isolated polypeptide comprising an amino acid sequence at least 95% identical to a sequence of at least about 30 contiguous amino acids in the amino acid sequence of a polypeptide encoded by the cDNA contained in ATCC™ Deposit No:Z.

Also preferred is an isolated polypeptide comprising an amino acid sequence at least 95% identical to a sequence of at least about 100 contiguous amino acids in the amino acid sequence of a polypeptide encoded by cDNA contained in ATCC™ Deposit No:Z.

Also preferred is an isolated polypeptide comprising an amino acid sequence at least 95% identical to the amino acid sequence of a polypeptide encoded by the cDNA contained in ATCC™ Deposit No:Z.

Further preferred is an isolated antibody which binds specifically to a polypeptide comprising an amino acid sequence that is at least 90% identical to a sequence of at least 10 contiguous amino acids in a sequence selected from the group consisting of: a polypeptide sequence of SEQ ID NO:Y; a polypeptide encoded by SEQ ID NO:X or the complementary strand thereto; the polypeptide encoded by the nucleotide sequence as defined in columns 8 and 9 of Table 2; and a polypeptide encoded by the cDNA contained in ATCC™ Deposit No:Z.

Further preferred is a method for detecting in a biological sample a polypeptide comprising an amino acid sequence which is at least 90% identical to a sequence of at least 10 contiguous amino acids in a sequence selected from the group consisting of: a polypeptide sequence of SEQ ID NO:Y; a polypeptide encoded by SEQ ID NO:X or the complementary strand thereto; the polypeptide encoded by the nucleotide sequence as defined in columns 8 and 9 of Table 2; and a polypeptide encoded by the cDNA contained in ATCC™ Deposit No:Z; which method comprises a step of comparing an amino acid sequence of at least one polypeptide molecule in said sample with a sequence selected from said group and determining whether the sequence of said polypeptide molecule in said sample is at least 90% identical to said sequence of at least 10 contiguous amino acids.

Also preferred is the above method wherein said step of comparing an amino acid sequence of at least one polypeptide molecule in said sample with a sequence selected from said group comprises determining the extent of specific binding of polypeptides in said sample to an antibody which binds specifically to a polypeptide comprising an amino acid sequence that is at least 90% identical to a sequence of at least 10 contiguous amino acids in a sequence selected from the group consisting of: a polypeptide sequence of SEQ ID NO:Y; a polypeptide encoded by SEQ ID NO:X or the complementary strand thereto; the polypeptide encoded by the nucleotide sequence as defined in columns 8 and 9 of Table 2; and a polypeptide encoded by the cDNA contained in ATCC™ Deposit No:Z.

Also preferred is the above method wherein said step of comparing sequences is performed by comparing the amino acid sequence determined from a polypeptide molecule in said sample with said sequence selected from said group.

Also preferred is a method for identifying the species, tissue or cell type of a biological sample which method comprises a step of detecting polypeptide molecules in said sample, if any, comprising an amino acid sequence that is at least 90% identical to a sequence of at least 10 contiguous amino acids in a sequence selected from the group consisting of: polypeptide sequence of SEQ ID NO:Y; a polypeptide encoded by SEQ ID NO:X or the complementary strand thereto; the polypeptide encoded by the nucleotide sequence as defined in columns 8 and 9 of Table 2; and a polypeptide encoded by the cDNA contained in ATCC™ Deposit No:Z.

Also preferred is the above method for identifying the species, tissue or cell type of a biological sample, which method comprises a step of detecting polypeptide molecules comprising an amino acid sequence in a panel of at least two amino acid sequences, wherein at least one sequence in said panel is at least 90% identical to a sequence of at least 10 contiguous amino acids in a sequence selected from the above group.

Also preferred is a method for diagnosing in a subject a pathological condition associated with abnormal structure or expression of a nucleic acid sequence identified in Table 1A, 1B or Table 2 encoding a polypeptide, which method comprises a step of detecting in a biological sample obtained from said subject polypeptide molecules comprising an amino acid sequence in a panel of at least two amino acid sequences, wherein at least one sequence in said panel is at least 90% identical to a sequence of at least 10 contiguous amino acids in a sequence selected from the group consisting of: polypeptide sequence of SEQ ID NO:Y; a polypeptide encoded by SEQ ID NO:X or the complementary strand thereto; the polypeptide encoded by the nucleotide sequence as defined in columns 8 and 9 of Table 2; and a polypeptide encoded by the cDNA contained in ATCC™ Deposit No:Z.

In any of these methods, the step of detecting said polypeptide molecules includes using an antibody.

Also preferred is an isolated nucleic acid molecule comprising a nucleotide sequence which is at least 95% identical to a nucleotide sequence encoding a polypeptide wherein said polypeptide comprises an amino acid sequence that is at least 90% identical to a sequence of at least 10 contiguous amino acids in a sequence selected from the group consisting of: polypeptide sequence of SEQ ID NO:Y; a polypeptide encoded by SEQ ID NO:X or the complementary strand thereto; the polypeptide encoded by the nucleotide sequence as defined in columns 8 and 9 of Table 2; and a polypeptide encoded by the cDNA contained in ATCC™ Deposit No:Z.

Also preferred is an isolated nucleic acid molecule, wherein said nucleotide sequence encoding a polypeptide has been optimized for expression of said polypeptide in a prokaryotic host.

Also preferred is a polypeptide molecule, wherein said polypeptide comprises an amino acid sequence selected from the group consisting of: polypeptide sequence of SEQ ID NO:Y; a polypeptide encoded by SEQ ID NO:X or the complementary strand thereto; the polypeptide encoded by the nucleotide sequence as defined in columns 8 and 9 of Table 2; and a polypeptide encoded by the cDNA contained in ATCC™ Deposit No:Z.

Further preferred is a method of making a recombinant vector comprising inserting any of the above isolated nucleic acid molecule into a vector. Also preferred is the recombinant vector produced by this method. Also preferred is a method of making a recombinant host cell comprising introducing the vector into a host cell, as well as the recombinant host cell produced by this method.

Also preferred is a method of making an isolated polypeptide comprising culturing this recombinant host cell under conditions such that said polypeptide is expressed and recovering said polypeptide. Also preferred is this method of making an isolated polypeptide, wherein said recombinant host cell is a eukaryotic cell and said polypeptide is a human protein comprising an amino acid sequence selected from the group consisting of: polypeptide sequence of SEQ ID NO:Y; a polypeptide encoded by SEQ ID NO:X or the complementary strand thereto; the polypeptide encoded by the nucleotide sequence as defined in columns 8 and 9 of Table 2; and a polypeptide encoded by the cDNA contained in ATCC™ Deposit No:Z. The isolated polypeptide produced by this method is also preferred.

Also preferred is a method of treatment of an individual in need of an increased level of a protein activity, which method comprises administering to such an individual a Therapeutic comprising an amount of an isolated polypeptide, polynucleotide, immunogenic fragment or analogue thereof, binding agent, antibody, or antigen binding fragment of the claimed invention effective to increase the level of said protein activity in said individual.

Also preferred is a method of treatment of an individual in need of a decreased level of a protein activity, which method comprised administering to such an individual a Therapeutic comprising an amount of an isolated polypeptide, polynucleotide, immunogenic fragment or analogue thereof, binding agent, antibody, or antigen binding fragment of the claimed invention effective to decrease the level of said protein activity in said individual.

Also preferred is a method of treatment of an individual in need of a specific delivery of toxic compositions to diseased cells (e.g., tumors, leukemias or lymphomas), which method comprises administering to such an individual a Therapeutic comprising an amount of an isolated polypeptide of the invention, including, but not limited to a binding agent, or antibody of the claimed invention that are associated with toxin or cytotoxic prodrugs.

Having generally described the invention, the same will be more readily understood by reference to the following examples, which are provided by way of illustration and are not intended as limiting.

Description of Table 6

Table 6 summarizes some of the ATCC™ Deposits, Deposit dates, and ATCC™ designation numbers of deposits made with the ATCC™ in connection with the present application. These deposits were made in addition to those described in the Table 1A.

Table 6ATCC™ Deposits Deposit Date ATCC™ Designation Number LP01, LP02, LP03, LP04, May-20-97 209059, 209060, 209061, 209062, 209063, LP05, LP06, LP07, LP08, 209064, 209065, 209066, 209067, 209068, LP09, LP 10, LP 11, 209069 LP 12 Jan-12-98 209579 LP13 Jan-12-98 209578 LP14 Jul-16-98 203067 LP15 Jul-16-98 203068 LP16 Feb-1-99 203609 LP17 Feb-1-99 203610 LP20 Nov-17-98 203485 LP21 Jun-18-99 PTA-252 LP22 Jun-18-99 PTA-253 LP23 Dec-22-99 PTA-1081

EXAMPLES Example 1 Isolation of a Selected cDNA Clone From the Deposited Sample

Each ATCC™ Deposit No:Z is contained in a plasmid vector. Table 7 identifies the vectors used to construct the cDNA library from which each clone was isolated. In many cases, the vector used to construct the library is a phage vector from which a plasmid has been excised. The following correlates the related plasmid for each phage vector used in constructing the cDNA library. For example, where a particular clone is identified in Table 7 as being isolated in the vector “Lambda Zap,” the corresponding deposited clone is in “pBLUESCRIPT™.” Vector Used to Construct Library Corresponding Deposited Plasmid Lambda Zap pBLUESCRIPT ™ (pBS) Uni-Zap XR pBLUESCRIPT ™ (pBS) Zap Express pBK lafmid BA plafmid BA pSport 1 pSport 1 pCMVSport 2.0 pCMVSport 2.0 pCMVSport 3.0 pCMVSport 3.0 pCR ® 2.1 pCR ® 2.1

Vectors Lambda Zap (U.S. Pat. Nos. 5,128,256 and 5,286,636), Uni-Zap XR (U.S. Pat. Nos. 5,128,256 and 5,286,636), Zap Express (U.S. Pat. Nos. 5,128,256 and 5,286,636), pBLUESCRIPT™ (pBS) (Short, J. M. et al., Nucleic Acids Res. 16:7583-7600 (1988); Alting-Mees, M. A. and Short, J. M., Nucleic Acids Res. 17:9494 (1989)) and pBK (Alting-Mees, M. A. et al., Strategies 5:58-61 (1992)) are commercially available from STRATAGENE™ Cloning Systems, Inc., 11011 N. Torrey Pines Road, La Jolla, Calif., 92037. pBS contains an ampicillin resistance gene and pBK contains a neomycin resistance gene. Both can be transformed into E. coli strain XL-1 Blue, also available from STRATAGENE™. pBS comes in 4 forms SK+, SK−, KS+ and KS. The S and K refers to the orientation of the polylinker to the T7 and T3 primer sequences which flank the polylinker region (“S” is for SacI and “K” is for KpnI which are the first sites on each respective end of the linker). “+” or “−” refer to the orientation of the f1 origin of replication (“ori”), such that in one orientation, single stranded rescue initiated from the f1 ori generates sense strand DNA and in the other, antisense.

Vectors pSport1, pCMVSport 2.0 and pCMVSport 3.0, were obtained from LIFE TECHNOLOGIES™, Inc., P.O. Box 6009, Gaithersburg, Md. 20897. All Sport vectors contain an ampicillin resistance gene and may be transformed into E. coli strain DH10B, also available from LIFE TECHNOLOGIES™. (See, for instance, Gruber, C. E., et al., Focus 15:59 (1993)). Vector lafmid BA (Bento Soares, Columbia University, NY) contains an ampicillin resistance gene and can be transformed into E. coli strain XL-1 Blue. Vector pCR®2.1, which is available from Invitrogen, 1600 Faraday Avenue, Carlsbad, Calif. 92008, contains an ampicillin resistance gene and may be transformed into E. coli strain DH10B, available from LIFE TECHNOLOGIES™. (See, for instance, Clark, J. M., Nuc. Acids Res. 16:9677-9686 (1988) and Mead, D. et al., Bio/Technology 9: (1991)). Preferably, a polynucleotide of the present invention does not comprise the phage vector sequences identified for the particular clone in Table 7, as well as the corresponding plasmid vector sequences designated above.

The deposited material in the sample assigned the ATCC™ Deposit Number cited by reference to Table 1A, Table 2, Table 6 and Table 7 for any given cDNA clone also may contain one or more additional plasmids, each comprising a cDNA clone different from that given clone. Thus, deposits sharing the same ATCC™ Deposit Number contain at least a plasmid for each ATCC™ Deposit No:Z. TABLE 7 ATCC ™ Libraries owned by Catalog Catalog Description Vector Deposit HUKA HUKB HUKC HUKD Human Uterine Cancer Lambda ZAP II LP01 HUKE HUKF HUKG HCNA HCNB Human Colon Lambda Zap II LP01 HFFA Human Fetal Brain, random Lambda Zap II LP01 primed HTWA Resting T-Cell Lambda ZAP II LP01 HBQA Early Stage Human Brain, Lambda ZAP II LP01 random primed HLMB HLMF HLMG HLMH breast lymph node CDNA Lambda ZAP II LP01 HLMI HLMJ HLMM HLMN library HCQA HCQB human colon cancer Lamda ZAP II LP01 HMEA HMEC HMED HMEE Human Microvascular Lambda ZAP II LP01 HMEF HMEG HMEI HMEJ Endothelial Cells, fract. A HMEK HMEL HUSA HUSC Human Umbilical Vein Lambda ZAP II LP01 Endothelial Cells, fract. A HLQA HLQB Hepatocellular Tumor Lambda ZAP II LP01 HHGA HHGB HHGC HHGD Hemangiopericytoma Lambda ZAP II LP01 HSDM Human Striatum Depression, re- Lambda ZAP II LP01 rescue HUSH H Umbilical Vein Endothelial Lambda ZAP II LP01 Cells, frac A, re-excision HSGS Salivary gland, subtracted Lambda ZAP II LP01 HFXA HFXB HFXC HFXD Brain frontal cortex Lambda ZAP II LP01 HFXE HFXF HFXG HFXH HPQA HPQB HPQC PERM TF274 Lambda ZAP II LP01 HFXJ HFXK Brain Frontal Cortex, re-excision Lambda ZAP II LP01 HCWA HCWB HCWC HCWD CD34 positive cells (Cord ZAP Express LP02 HCWE HCWF HCWG HCWH Blood) HCWI HCWJ HCWK HCUA HCUB HCUC CD34 depleted Buffy Coat ZAP Express LP02 (Cord Blood) HRSM A-14 cell line ZAP Express LP02 HRSA A1-CELL LINE ZAP Express LP02 HCUD HCUE HCUF HCUG CD34 depleted Buffy Coat ZAP Express LP02 HCUH HCUI (Cord Blood), re-excision HBXE HBXF HBXG H. Whole Brain #2, re-excision ZAP Express LP02 HRLM L8 cell line ZAP Express LP02 HBXA HBXB HBXC HBXD Human Whole Brain #2 - Oligo ZAP Express LP02 dT > 1.5 Kb HUDA HUDB HUDC Testes ZAP Express LP02 HHTM HHTN HHTO H. hypothalamus, frac A; re- ZAP Express LP02 excision HHTL H. hypothalamus, frac A ZAP Express LP02 HASA HASD Human Adult Spleen Uni-ZAP XR LP03 HFKC HFKD HFKE HFKF Human Fetal Kidney Uni-ZAP XR LP03 HFKG HE8A HE8B HE8C HE8D Human 8 Week Whole Embryo Uni-ZAP XR LP03 HE8E HE8F HE8M HE8N HGBA HGBD HGBE HGBF Human Gall Bladder Uni-ZAP XR LP03 HGBG HGBH HGBI HLHA HLHB HLHC HLHD Human Fetal Lung III Uni-ZAP XR LP03 HLHE HLHF HLHG HLHH HLHQ HPMA HPMB HPMC HPMD Human Placenta Uni-ZAP XR LP03 HPME HPMF HPMG HPMH HPRA HPRB HPRC HPRD Human Prostate Uni-ZAP XR LP03 HSIA HSIC HSID HSIE Human Adult Small Intestine Uni-ZAP XR LP03 HTEA HTEB HTEC HTED Human Testes Uni-ZAP XR LP03 HTEE HTEF HTEG HTEH HTEI HTEJ HTEK HTPA HTPB HTPC HTPD Human Pancreas Tumor Uni-ZAP XR LP03 HTPE HTTA HTTB HTTC HTTD Human Testes Tumor Uni-ZAP XR LP03 HTTE HTTF HAPA HAPB HAPC HAPM Human Adult Pulmonary Uni-ZAP XR LP03 HETA HETB HETC HETD Human Endometrial Tumor Uni-ZAP XR LP03 HETE HETF HETG HETH HETI HHFB HHFC HHFD HHFE Human Fetal Heart Uni-ZAP XR LP03 HHFF HHFG HHFH HHFI HHPB HHPC HHPD HHPE Human Hippocampus Uni-ZAP XR LP03 HHPF HHPG HHPH HCE1 HCE2 HCE3 HCE4 Human Cerebellum Uni-ZAP XR LP03 HCE5 HCEB HCEC HCED HCEE HCEF HCEG HUVB HUVC HUVD HUVE Human Umbilical Vein, Endo. Uni-ZAP XR LP03 remake HSTA HSTB HSTC HSTD Human Skin Tumor Uni-ZAP XR LP03 HTAA HTAB HTAC HTAD Human Activated T-Cells Uni-ZAP XR LP03 HTAE HFEA HFEB HFEC Human Fetal Epithelium (Skin) Uni-ZAP XR LP03 HJPA HJPB HJPC HJPD HUMAN JURKAT Uni-ZAP XR LP03 MEMBRANE BOUND POLYSOMES HESA Human epithelioid sarcoma Uni-Zap XR LP03 HLTA HLTB HLTC HLTD Human T-Cell Lymphoma Uni-ZAP XR LP03 HLTE HLTF HFTA HFTB HFTC HFTD Human Fetal Dura Mater Uni-ZAP XR LP03 HRDA HRDB HRDC HRDD Human Rhabdomyosarcoma Uni-ZAP XR LP03 HRDE HRDF HCAA HCAB HCAC Cem cells cyclohexamide treated Uni-ZAP XR LP03 HRGA HRGB HRGC HRGD Raji Cells, cyclohexamide Uni-ZAP XR LP03 treated HSUA HSUB HSUC HSUM Supt Cells, cyclohexamide Uni-ZAP XR LP03 treated HT4A HT4C HT4D Activated T-Cells, 12 hrs. Uni-ZAP XR LP03 HE9A HE9B HE9C HE9D Nine Week Old Early Stage Uni-ZAP XR LP03 HE9E HE9F HE9G HE9H Human HE9M HE9N HATA HATB HATC HATD Human Adrenal Gland Tumor Uni-ZAP XR LP03 HATE HT5A Activated T-Cells, 24 hrs. Uni-ZAP XR LP03 HFGA HFGM Human Fetal Brain Uni-ZAP XR LP03 HNEA HNEB HNEC HNED Human Neutrophil Uni-ZAP XR LP03 HNEE HBGB HBGD Human Primary Breast Cancer Uni-ZAP XR LP03 HBNA HBNB Human Normal Breast Uni-ZAP XR LP03 HCAS Cem Cells, cyclohexamide Uni-ZAP XR LP03 treated, subtra HHPS Human Hippocampus, pBS LP03 subtracted HKCS HKCU Human Colon Cancer, pBS LP03 subtracted HRGS Raji cells, cyclohexamide pBS LP03 treated, subtracted HSUT Supt cells, cyclohexamide pBS LP03 treated, differentially expressed HT4S Activated T-Cells, 12 hrs, Uni-ZAP XR LP03 subtracted HCDA HCDB HCDC HCDD Human Chondrosarcoma Uni-ZAP XR LP03 HCDE HOAA HOAB HOAC Human Osteosarcoma Uni-ZAP XR LP03 HTLA HTLB HTLC HTLD Human adult testis, large inserts Uni-ZAP XR LP03 HTLE HTLF HLMA HLMC HLMD Breast Lymph node cDNA Uni-ZAP XR LP03 library H6EA H6EB H6EC HL-60, PMA 4 H Uni-ZAP XR LP03 HTXA HTXB HTXC HTXD Activated T-Cell Uni-ZAP XR LP03 HTXE HTXF HTXG HTXH (12 hs)/Thiouridine labelledEco HNFA HNFB HNFC HNFD Human Neutrophil, Activated Uni-ZAP XR LP03 HNFE HNFF HNFG HNFH HNFJ HTOB HTOC HUMAN TONSILS, Uni-ZAP XR LP03 FRACTION 2 HMGB Human OB MG63 control Uni-ZAP XR LP03 fraction I HOPB Human OB HOS control fraction I Uni-ZAP XR LP03 HORB Human OB HOS treated (10 nM Uni-ZAP XR LP03 E2) fraction I HSVA HSVB HSVC Human Chronic Synovitis Uni-ZAP XR LP03 HROA HUMAN STOMACH Uni-ZAP XR LP03 HBJA HBJB HBJC HBJD HBJE HUMAN B CELL Uni-ZAP XR LP03 HBJF HBJG HBJH HBJI HBJJ LYMPHOMA HBJK HCRA HCRB HCRC human corpus colosum Uni-ZAP XR LP03 HODA HODB HODC HODD human ovarian cancer Uni-ZAP XR LP03 HDSA Dermatofibrosarcoma Uni-ZAP XR LP03 Protuberance HMWA HMWB HMWC Bone Marrow Cell Line Uni-ZAP XR LP03 HMWD HMWE HMWF (RS4; 11) HMWG HMWH HMWI HMWJ HSOA stomach cancer (human) Uni-ZAP XR LP03 HERA SKIN Uni-ZAP XR LP03 HMDA Brain-medulloblastoma Uni-ZAP XR LP03 HGLA HGLB HGLD Glioblastoma Uni-ZAP XR LP03 HEAA H. Atrophic Endometrium Uni-ZAP XR LP03 HBCA HBCB H. Lymph node breast Cancer Uni-ZAP XR LP03 HPWT Human Prostate BPH, re- Uni-ZAP XR LP03 excision HFVG HFVH HFVI Fetal Liver, subtraction II pBS LP03 HNFI Human Neutrophils, Activated, pBS LP03 re-excision HBMB HBMC HBMD Human Bone Marrow, re- pBS LP03 excision HKML HKMM HKMN H. Kidney Medulla, re-excision pBS LP03 HKIX HKIY H. Kidney Cortex, subtracted pBS LP03 HADT H. Amygdala Depression, pBS LP03 subtracted H6AS Hl-60, untreated, subtracted Uni-ZAP XR LP03 H6ES HL-60, PMA 4 H, subtracted Uni-ZAP XR LP03 H6BS HL-60, RA 4 h, Subtracted Uni-ZAP XR LP03 H6CS HL-60, PMA 1 d, subtracted Uni-ZAP XR LP03 HTXJ HTXK Activated T- Uni-ZAP XR LP03 cell(12 h)/Thiouridine-re- excision HMSA HMSB HMSC HMSD Monocyte activated Uni-ZAP XR LP03 HMSE HMSF HMSG HMSH HMSI HMSJ HMSK HAGA HAGB HAGC HAGD Human Amygdala Uni-ZAP XR LP03 HAGE HAGF HSRA HSRB HSRE STROMAL- Uni-ZAP XR LP03 OSTEOCLASTOMA HSRD HSRF HSRG HSRH Human Osteoclastoma Stromal Uni-ZAP XR LP03 Cells - unamplified HSQA HSQB HSQC HSQD Stromal cell TF274 Uni-ZAP XR LP03 HSQE HSQF HSQG HSKA HSKB HSKC HSKD Smooth muscle, serum treated Uni-ZAP XR LP03 HSKE HSKF HSKZ HSLA HSLB HSLC HSLD Smooth muscle, control Uni-ZAP XR LP03 HSLE HSLF HSLG HSDA HSDD HSDE HSDF Spinal cord Uni-ZAP XR LP03 HSDG HSDH HPWS Prostate-BPH subtracted II pBS LP03 HSKW HSKX HSKY Smooth Muscle-HASTE pBS LP03 normalized HFPB HFPC HFPD H. Frontal cortex, epileptic; re- Uni-ZAP XR LP03 excision HSDI HSDJ HSDK Spinal Cord, re-excision Uni-ZAP XR LP03 HSKN HSKO Smooth Muscle Serum Treated, pBS LP03 Norm HSKG HSKH HSKI Smooth muscle, serum pBS LP03 induced, re-exc HFCA HFCB HFCC HFCD Human Fetal Brain Uni-ZAP XR LP04 HFCE HFCF HPTA HPTB HPTD Human Pituitary Uni-ZAP XR LP04 HTHB HTHC HTHD Human Thymus Uni-ZAP XR LP04 HE6B HE6C HE6D HE6E HE6F Human Whole Six Week Old Uni-ZAP XR LP04 HE6G HE6S Embryo HSSA HSSB HSSC HSSD Human Synovial Sarcoma Uni-ZAP XR LP04 HSSE HSSF HSSG HSSH HSSI HSSJ HSSK HE7T 7 Week Old Early Stage Human, Uni-ZAP XR LP04 subtracted HEPA HEPB HEPC Human Epididymus Uni-ZAP XR LP04 HSNA HSNB HSNC HSNM Human Synovium Uni-ZAP XR LP04 HSNN HPFB HPFC HPFD HPFE Human Prostate Cancer, Stage C Uni-ZAP XR LP04 fraction HE2A HE2D HE2E HE2H HE2I 12 Week Old Early Stage Uni-ZAP XR LP04 HE2M HE2N HE2O Human HE2B HE2C HE2F HE2G HE2P 12 Week Old Early Stage Uni-ZAP XR LP04 HE2Q Human, II HPTS HPTT HPTU Human Pituitary, subtracted Uni-ZAP XR LP04 HAUA HAUB HAUC Amniotic Cells - TNF induced Uni-ZAP XR LP04 HAQA HAQB HAQC HAQD Amniotic Cells - Primary Uni-ZAP XR LP04 Culture HWTA HWTB HWTC wilm's tumor Uni-ZAP XR LP04 HBSD Bone Cancer, re-excision Uni-ZAP XR LP04 HSGB Salivary gland, re-excision Uni-ZAP XR LP04 HSJA HSJB HSJC Smooth muscle-ILb induced Uni-ZAP XR LP04 HSXA HSXB HSXC HSXD Human Substantia Nigra Uni-ZAP XR LP04 HSHA HSHB HSHC Smooth muscle, IL1b induced Uni-ZAP XR LP04 HOUA HOUB HOUC HOUD Adipocytes Uni-ZAP XR LP04 HOUE HPWA HPWB HPWC HPWD Prostate BPH Uni-ZAP XR LP04 HPWE HELA HELB HELC HELD Endothelial cells-control Uni-ZAP XR LP04 HELE HELF HELG HELH HEMA HEMB HEMC HEMD Endothelial-induced Uni-ZAP XR LP04 HEME HEMF HEMG HEMH HBIA HBIB HBIC Human Brain, Striatum Uni-ZAP XR LP04 HHSA HHSB HHSC HHSD Human Uni-ZAP XR LP04 HHSE Hypothalmus, Schizophrenia HNGA HNGB HNGC HNGD neutrophils control Uni-ZAP XR LP04 HNGE HNGF HNGG HNGH HNGI HNGJ HNHA HNHB HNHC HNHD Neutrophils IL-1 and LPS Uni-ZAP XR LP04 HNHE HNHF HNHG HNHH induced HNHI HNHJ HSDB HSDC STRIATUM DEPRESSION Uni-ZAP XR LP04 HHPT Hypothalamus Uni-ZAP XR LP04 HSAT HSAU HSAV HSAW Anergic T-cell Uni-ZAP XR LP04 HSAX HSAY HSAZ HBMS HBMT HBMU HBMV Bone marrow Uni-ZAP XR LP04 HBMW HBMX HOEA HOEB HOEC HOED Osteoblasts Uni-ZAP XR LP04 HOEE HOEF HOEJ HAIA HAIB HAIC HAID HAIE Epithelial-TNFa and INF Uni-ZAP XR LP04 HAIF induced HTGA HTGB HTGC HTGD Apoptotic T-cell Uni-ZAP XR LP04 HMCA HMCB HMCC HMCD Macrophage-oxLDL Uni-ZAP XR LP04 HMCE HMAA HMAB HMAC HMAD Macrophage (GM-CSF treated) Uni-ZAP XR LP04 HMAE HMAF HMAG HPHA Normal Prostate Uni-ZAP XR LP04 HPIA HPIB HPIC LNCAP prostate cell line Uni-ZAP XR LP04 HPJA HPJB HPJC PC3 Prostate cell line Uni-ZAP XR LP04 HOSE HOSF HOSG Human Osteoclastoma, re- Uni-ZAP XR LP04 excision HTGE HTGF Apoptotic T-cell, re-excision Uni-ZAP XR LP04 HMAJ HMAK H Macrophage (GM-CSF Uni-ZAP XR LP04 treated), re-excision HACB HACC HACD Human Adipose Tissue, re- Uni-ZAP XR LP04 excision HFPA H. Frontal Cortex, Epileptic Uni-ZAP XR LP04 HFAA HFAB HFAC HFAD Alzheimer's, spongy change Uni-ZAP XR LP04 HFAE HFAM Frontal Lobe, Dementia Uni-ZAP XR LP04 HMIA HMIB HMIC Human Manic Depression Uni-ZAP XR LP04 Tissue HTSA HTSE HTSF HTSG Human Thymus pBS LP05 HTSH HPBA HPBB HPBC HPBD Human Pineal Gland pBS LP05 HPBE HSAA HSAB HSAC HSA 172 Cells pBS LP05 HSBA HSBB HSBC HSBM HSC172 cells pBS LP05 HJAA HJAB HJAC HJAD Jurkat T-cell G1 phase pBS LP05 HJBA HJBB HJBC HJBD Jurkat T-Cell, S phase pBS LP05 HAFA HAFB Aorta endothelial cells + TNF-a pBS LP05 HAWA HAWB HAWC Human White Adipose pBS LP05 HTNA HTNB Human Thyroid pBS LP05 HONA Normal Ovary, Premenopausal pBS LP05 HARA HARB Human Adult Retina pBS LP05 HLJA HLJB Human Lung pCMVSport 1 LP06 HOFM HOFN HOFO H. Ovarian Tumor, II, OV5232 pCMVSport 2.0 LP07 HOGA HOGB HOGC OV 10-3-95 pCMVSport 2.0 LP07 HCGL CD34+cells, II pCMVSport 2.0 LP07 HDLA Hodgkin's Lymphoma I pCMVSport 2.0 LP07 HDTA HDTB HDTC HDTD Hodgkin's Lymphoma II pCMVSport 2.0 LP07 HDTE HKAA HKAB HKAC HKAD Keratinocyte pCMVSport 2.0 LP07 HKAE HKAF HKAG HKAH HCIM CAPFINDER, Crohn's Disease, pCMVSport 2.0 LP07 lib 2 HKAL Keratinocyte, lib 2 pCMVSport 2.0 LP07 HKAT Keratinocyte, lib 3 pCMVSport 2.0 LP07 HNDA Nasal polyps pCMVSport 2.0 LP07 HDRA H. Primary Dendritic Cells, lib 3 pCMVSport 2.0 LP07 HOHA HOHB HOHC Human Osteoblasts II pCMVSport 2.0 LP07 HLDA HLDB HLDC Liver, Hepatoma pCMVSport 3.0 LP08 HLDN HLDO HLDP Human Liver, normal pCMVSport 3.0 LP08 HMTA pBMC stimulated w/ poly I/C pCMVSport 3.0 LP08 HNTA NTERA2, control pCMVSport 3.0 LP08 HDPA HDPB HDPC HDPD Primary Dendritic Cells, lib 1 pCMVSport 3.0 LP08 HDPF HDPG HDPH HDPI HDPJ HDPK HDPM HDPN HDPO HDPP Primary Dendritic cells, frac 2 pCMVSport 3.0 LP08 HMUA HMUB HMUC Myoloid Progenitor Cell Line pCMVSport 3.0 LP08 HHEA HHEB HHEC HHED T Cell helper I pCMVSport 3.0 LP08 HHEM HHEN HHEO HHEP T cell helper II pCMVSport 3.0 LP08 HEQA HEQB HEQC Human endometrial stromal cells pCMVSport 3.0 LP08 HJMA HJMB Human endometrial stromal pCMVSport 3.0 LP08 cells-treated with progesterone HSWA HSWB HSWC Human endometrial stromal pCMVSport 3.0 LP08 cells-treated with estradiol HSYA HSYB HSYC Human Thymus Stromal Cells pCMVSport 3.0 LP08 HLWA HLWB HLWC Human Placenta pCMVSport 3.0 LP08 HRAA HRAB HRAC Rejected Kidney, lib 4 pCMVSport 3.0 LP08 HMTM PCR, pBMC I/C treated PCRII LP09 HMJA H. Meniingima, M6 pSport 1 LP10 HMKA HMKB HMKC HMKD H. Meningima, M1 pSport 1 LP10 HMKE HUSG HUSI Human umbilical vein pSport 1 LP10 endothelial cells, IL-4 induced HUSX HUSY Human Umbilical Vein pSport 1 LP10 Endothelial Cells, uninduced HOFA Ovarian Tumor I, OV5232 pSport 1 LP10 HCFA HCFB HCFC HCFD T-Cell PHA 16 hrs pSport 1 LP10 HCFL HCFM HCFN HCFO T-Cell PHA 24 hrs pSport 1 LP10 HADA HADC HADD HADE Human Adipose pSport 1 LP10 HADF HADG HOVA HOVB HOVC Human Ovary pSport 1 LP10 HTWB HTWC HTWD HTWE Resting T-Cell Library, II pSport 1 LP10 HTWF HMMA Spleen metastic melanoma pSport 1 LP10 HLYA HLYB HLYC HLYD Spleen, Chronic lymphocytic pSport 1 LP10 HLYE leukemia HCGA CD34+ cell, I pSport 1 LP10 HEOM HEON Human Eosinophils pSport 1 LP10 HTDA Human Tonsil, Lib 3 pSport 1 LP10 HSPA Salivary Gland, Lib 2 pSport 1 LP10 HCHA HCHB HCHC Breast Cancer cell line, MDA 36 pSport 1 LP10 HCHM HCHN Breast Cancer Cell line, pSport 1 LP10 angiogenic HCIA Crohn's Disease pSport 1 LP10 HDAA HDAB HDAC HEL cell line pSport 1 LP10 HABA Human Astrocyte pSport 1 LP10 HUFA HUFB HUFC Ulcerative Colitis pSport 1 LP10 HNTM NTERA2 + retinoic acid, 14 pSport 1 LP10 days HDQA Primary Dendritic pSport 1 LP10 cells, CapFinder2, frac 1 HDQM Primary Dendritic Cells, pSport 1 LP10 CapFinder, frac 2 HLDX Human Liver, normal, CapFinder pSport 1 LP10 HULA HULB HULC Human Dermal Endothelial pSport 1 LP10 Cells, untreated HUMA Human Dermal Endothelial pSport 1 LP10 cells, treated HCJA Human Stromal Endometrial pSport 1 LP10 fibroblasts, untreated HCJM Human Stromal endometrial pSport 1 LP10 fibroblasts, treated w/ estradiol HEDA Human Stromal endometrial pSport 1 LP10 fibroblasts, treated with progesterone HFNA Human ovary tumor cell pSport 1 LP10 OV350721 HKGA HKGB HKGC HKGD Merkel Cells pSport 1 LP10 HISA HISB HISC Pancreas Islet Cell Tumor pSport 1 LP10 HLSA Skin, burned pSport 1 LP10 HBZA Prostate, BPH, Lib 2 pSport 1 LP10 HBZS Prostate BPH, Lib 2, subtracted pSport 1 LP10 HFIA HFIB HFIC Synovial Fibroblasts (control) pSport 1 LP10 HFIH HFII HFIJ Synovial hypoxia pSport 1 LP10 HFIT HFIU HFIV Synovial IL-1/TNF stimulated pSport 1 LP10 HGCA Messangial cell, frac 1 pSport 1 LP10 HMVA HMVB HMVC Bone Marrow Stromal Cell, pSport 1 LP10 untreated HFIX HFIY HFIZ Synovial Fibroblasts (Il1/TNF), pSport 1 LP10 subt HFOX HFOY HFOZ Synovial hypoxia-RSF pSport 1 LP10 subtracted HMQA HMQB HMQC HMQD Human Activated Monocytes Uni-ZAP XR LP11 HLIA HLIB HLIC Human Liver pCMVSport 1 LP012 HHBA HHBB HHBC HHBD Human Heart pCMVSport 1 LP012 HHBE HBBA HBBB Human Brain pCMVSport 1 LP012 HLJA HLJB HLJC HLJD HLJE Human Lung pCMVSport 1 LP012 HOGA HOGB HOGC Ovarian Tumor pCMVSport 2.0 LP012 HTJM Human Tonsils, Lib 2 pCMVSport 2.0 LP012 HAMF HAMG KMH2 pCMVSport 3.0 LP012 HAJA HAJB HAJC L428 pCMVSport 3.0 LP012 HWBA HWBB HWBC HWBD Dendritic cells, pooled pCMVSport 3.0 LP012 HWBE HWAA HWAB HWAC HWAD Human Bone Marrow, treated pCMVSport 3.0 LP012 HWAE HYAA HYAB HYAC B Cell lymphoma pCMVSport 3.0 LP012 HWHG HWHH HWHI Healing groin wound, 6.5 hours pCMVSport 3.0 LP012 post incision HWHP HWHQ HWHR Healing groin wound; 7.5 hours pCMVSport 3.0 LP012 post incision HARM Healing groin wound - zero hr pCMVSport 3.0 LP012 post-incision (control) HBIM Olfactory epithelium; pCMVSport 3.0 LP012 nasalcavity HWDA Healing Abdomen wound; pCMVSport 3.0 LP012 70&90 min post incision HWEA Healing Abdomen Wound; 15 pCMVSport 3.0 LP012 days post incision HWJA Healing Abdomen pCMVSport 3.0 LP012 Wound; 21&29 days HNAL Human Tongue, frac 2 pSport 1 LP012 HMJA H. Meniingima, M6 pSport 1 LP012 HMKA HMKB HMKC HMKD H. Meningima, M1 pSport 1 LP012 HMKE HOFA Ovarian Tumor I, OV5232 pSport 1 LP012 HCFA HCFB HCFC HCFD T-Cell PHA 16 hrs pSport 1 LP012 HCFL HCFM HCFN HCFO T-Cell PHA 24 hrs pSport 1 LP012 HMMA HMMB HMMC Spleen metastic melanoma pSport 1 LP012 HTDA Human Tonsil, Lib 3 pSport 1 LP012 HDBA Human Fetal Thymus pSport 1 LP012 HDUA Pericardium pSport 1 LP012 HBZA Prostate, BPH, Lib 2 pSport 1 LP012 HWCA Larynx tumor pSport 1 LP012 HWKA Normal lung pSport 1 LP012 HSMB Bone marrow stroma, treated pSport 1 LP012 HBHM Normal trachea pSport 1 LP012 HLFC Human Larynx pSport 1 LP012 HLRB Siebben Polyposis pSport 1 LP012 HNIA Mammary Gland pSport 1 LP012 HNJB Palate carcinoma pSport 1 LP012 HNKA Palate normal pSport 1 LP012 HMZA Pharynx carcinoma pSport 1 LP012 HABG Cheek Carcinoma pSport 1 LP012 HMZM Pharynx Carcinoma pSport 1 LP012 HDRM Larynx Carcinoma pSport 1 LP012 HVAA Pancreas normal PCA4 No pSport 1 LP012 HICA Tongue carcinoma pSport 1 LP012 HUKA HUKB HUKC HUKD Human Uterine Cancer Lambda ZAP II LP013 HUKE HFFA Human Fetal Brain, random Lambda ZAP II LP013 primed HTUA Activated T-cell labeled with 4- Lambda ZAP II LP013 thioluri HBQA Early Stage Human Brain, Lambda ZAP II LP013 random primed HMEB Human microvascular Lambda ZAP II LP013 Endothelial cells, fract. B HUSH Human Umbilical Vein Lambda ZAP II LP013 Endothelial cells, fract. A, re- excision HLQC HLQD Hepatocellular tumor, re- Lambda ZAP II LP013 excision HTWJ HTWK HTWL Resting T-cell, re-excision Lambda ZAP II LP013 HF6S Human Whole 6 week Old pBLUESCRIPT ™ LP013 Embryo (II), subt HHPS Human Hippocampus, pBLUESCRIPT ™ LP013 subtracted HL1S LNCAP, differential expression pBLUESCRIPT ™ LP013 HLHS HLHT Early Stage Human Lung, pBLUESCRIPT ™ LP013 Subtracted HSUS Supt cells, cyclohexamide pBLUESCRIPT ™ LP013 treated, subtracted HSUT Supt cells, cyclohexamide pBLUESCRIPT ™ LP013 treated, differentially expressed HSDS H. Striatum Depression, pBLUESCRIPT ™ LP013 subtracted HPTZ Human Pituitary, Subtracted VII pBLUESCRIPT ™ LP013 HSDX H. Striatum Depression, subt II pBLUESCRIPT ™ LP013 HSDZ H. Striatum Depression, subt pBLUESCRIPT ™ LP013 HPBA HPBB HPBC HPBD Human Pineal Gland pBLUESCRIPT ™ LP013 HPBE SK− HRTA Colorectal Tumor pBLUESCRIPT ™ LP013 SK− HSBA HSBB HSBC HSBM HSC172 cells pBLUESCRIPT ™ LP013 SK− HJAA HJAB HJAC HJAD Jurkat T-cell G1 phase pBLUESCRIPT ™ LP013 SK− HJBA HJBB HJBC HJBD Jurkat T-cell, S1 phase pBLUESCRIPT ™ LP013 SK− HTNA HTNB Human Thyroid pBLUESCRIPT ™ LP013 SK− HAHA HAHB Human Adult Heart Uni-ZAP XR LP013 HE6A Whole 6 week Old Embryo Uni-ZAP XR LP013 HFCA HFCB HFCC HFCD Human Fetal Brain Uni-ZAP XR LP013 HFCE HFKC HFKD HFKE HFKF Human Fetal Kidney Uni-ZAP XR LP013 HFKG HGBA HGBD HGBE HGBF Human Gall Bladder Uni-ZAP XR LP013 HGBG HPRA HPRB HPRC HPRD Human Prostate Uni-ZAP XR LP013 HTEA HTEB HTEC HTED Human Testes Uni-ZAP XR LP013 HTEE HTTA HTTB HTTC HTTD Human Testes Tumor Uni-ZAP XR LP013 HTTE HYBA HYBB Human Fetal Bone Uni-ZAP XR LP013 HFLA Human Fetal Liver Uni-ZAP XR LP013 HHFB HHFC HHFD HHFE Human Fetal Heart Uni-ZAP XR LP013 HHFF HUVB HUVC HUVD HUVE Human Umbilical Vein, End. Uni-ZAP XR LP013 remake HTHB HTHC HTHD Human Thymus Uni-ZAP XR LP013 HSTA HSTB HSTC HSTD Human Skin Tumor Uni-ZAP XR LP013 HTAA HTAB HTAC HTAD Human Activated T-cells Uni-ZAP XR LP013 HTAE HFEA HFEB HFEC Human Fetal Epithelium (skin) Uni-ZAP XR LP013 HJPA HJPB HJPC HJPD Human Jurkat Membrane Bound Uni-ZAP XR LP013 Polysomes HESA Human Epithelioid Sarcoma Uni-ZAP XR LP013 HALS Human Adult Liver, Subtracted Uni-ZAP XR LP013 HFTA HFTB HFTC HFTD Human Fetal Dura Mater Uni-ZAP XR LP013 HCAA HCAB HCAC Cem cells, cyclohexamide Uni-ZAP XR LP013 treated HRGA HRGB HRGC HRGD Raji Cells, cyclohexamide Uni-ZAP XR LP013 treated HE9A HE9B HE9C HE9D Nine Week Old Early Stage Uni-ZAP XR LP013 HE9E Human HSFA Human Fibrosarcoma Uni-ZAP XR LP013 HATA HATB HATC HATD Human Adrenal Gland Tumor Uni-ZAP XR LP013 HATE HTRA Human Trachea Tumor Uni-ZAP XR LP013 HE2A HE2D HE2E HE2H HE2I 12 Week Old Early Stage Uni-ZAP XR LP013 Human HE2B HE2C HE2F HE2G HE2P 12 Week Old Early Stage Uni-ZAP XR LP013 Human, II HNEA HNEB HNEC HNED Human Neutrophil Uni-ZAP XR LP013 HNEE HBGA Human Primary Breast Cancer Uni-ZAP XR LP013 HPTS HPTT HPTU Human Pituitary, subtracted Uni-ZAP XR LP013 HMQA HMQB HMQC HMQD Human Activated Monocytes Uni-ZAP XR LP013 HOAA HOAB HOAC Human Osteosarcoma Uni-ZAP XR LP013 HTOA HTOD HTOE HTOF human tonsils Uni-ZAP XR LP013 HTOG HMGB Human OB MG63 control Uni-ZAP XR LP013 fraction I HOPB Human OB HOS control fraction I Uni-ZAP XR LP013 HOQB Human OB HOS treated (1 nM Uni-ZAP XR LP013 E2) fraction I HAUA HAUB HAUC Amniotic Cells - TNF induced Uni-ZAP XR LP013 HAQA HAQB HAQC HAQD Amniotic Cells - Primary Uni-ZAP XR LP013 Culture HROA HROC HUMAN STOMACH Uni-ZAP XR LP013 HBJA HBJB HBJC HBJD HBJE HUMAN B CELL Uni-ZAP XR LP013 LYMPHOMA HODA HODB HODC HODD human ovarian cancer Uni-ZAP XR LP013 HCPA Corpus Callosum Uni-ZAP XR LP013 HSOA stomach cancer (human) Uni-ZAP XR LP013 HERA SKIN Uni-ZAP XR LP013 HMDA Brain-medulloblastoma Uni-ZAP XR LP013 HGLA HGLB HGLD Glioblastoma Uni-ZAP XR LP013 HWTA HWTB HWTC wilm's tumor Uni-ZAP XR LP013 HEAA H. Atrophic Endometrium Uni-ZAP XR LP013 HAPN HAPO HAPP HAPQ Human Adult Pulmonary; re- Uni-ZAP XR LP013 HAPR excision HLTG HLTH Human T-cell lymphoma; re- Uni-ZAP XR LP013 excision HAHC HAHD HAHE Human Adult Heart; re-excision Uni-ZAP XR LP013 HAGA HAGB HAGC HAGD Human Amygdala Uni-ZAP XR LP013 HAGE HSJA HSJB HSJC Smooth muscle-ILb induced Uni-ZAP XR LP013 HSHA HSHB HSHC Smooth muscle, IL1b induced Uni-ZAP XR LP013 HPWA HPWB HPWC HPWD Prostate BPH Uni-ZAP XR LP013 HPWE HPIA HPIB HPIC LNCAP prostate cell line Uni-ZAP XR LP013 HPJA HPJB HPJC PC3 Prostate cell line Uni-ZAP XR LP013 HBTA Bone Marrow Stroma, Uni-ZAP XR LP013 TNF&LPS ind HMCF HMCG HMCH HMCI Macrophage-oxLDL; re-excision Uni-ZAP XR LP013 HMCJ HAGG HAGH HAGI Human Amygdala; re-excision Uni-ZAP XR LP013 HACA H. Adipose Tissue Uni-ZAP XR LP013 HKFB K562 + PMA (36 hrs), re- ZAP Express LP013 excision HCWT HCWU HCWV CD34 positive cells (cord ZAP Express LP013 blood), re-ex HBWA Whole brain ZAP Express LP013 HBXA HBXB HBXC HBXD Human Whole Brain #2 - Oligo ZAP Express LP013 dT >1.5 Kb HAVM Temporal cortex-Alzheizmer pT-Adv LP014 HAVT Hippocampus, Alzheimer pT-Adv LP014 Subtracted HHAS CHME Cell Line Uni-ZAP XR LP014 HAJR Larynx normal pSport 1 LP014 HWLE HWLF HWLG HWLH Colon Normal pSport 1 LP014 HCRM HCRN HCRO Colon Carcinoma pSport 1 LP014 HWLI HWLJ HWLK Colon Normal pSport 1 LP014 HWLQ HWLR HWLS HWLT Colon Tumor pSport 1 LP014 HBFM Gastrocnemius Muscle pSport 1 LP014 HBOD HBOE Quadriceps Muscle pSport 1 LP014 HBKD HBKE Soleus Muscle pSport 1 LP014 HCCM Pancreatic Langerhans pSport 1 LP014 HWGA Larynx carcinoma pSport 1 LP014 HWGM HWGN Larynx carcinoma pSport 1 LP014 HWLA HWLB HWLC Normal colon pSport 1 LP014 HWLM HWLN Colon Tumor pSport 1 LP014 HVAM HVAN HVAO Pancreas Tumor pSport 1 LP014 HWGQ Larynx carcinoma pSport 1 LP014 HAQM HAQN Salivary Gland pSport 1 LP014 HASM Stomach; normal pSport 1 LP014 HBCM Uterus; normal pSport 1 LP014 HCDM Testis; normal pSport 1 LP014 HDJM Brain; normal pSport 1 LP014 HEFM Adrenal Gland, normal pSport 1 LP014 HBAA Rectum normal pSport 1 LP014 HFDM Rectum tumour pSport 1 LP014 HGAM Colon, normal pSport 1 LP014 HHMM Colon, tumour pSport 1 LP014 HCLB HCLC Human Lung Cancer Lambda Zap II LP015 HRLA L1 Cell line ZAP Express LP015 HHAM Hypothalamus, Alzheimer's pCMVSport 3.0 LP015 HKBA Ku 812F Basophils Line pSport 1 LP015 HS2S Saos2, Dexamethosome Treated pSport 1 LP016 HA5A Lung Carcinoma A549 pSport 1 LP016 TNFalpha activated HTFM TF-1 Cell Line GM-CSF Treated pSport 1 LP016 HYAS Thyroid Tumour pSport 1 LP016 HUTS Larynx Normal pSport 1 LP016 HXOA Larynx Tumor pSport 1 LP016 HEAH Ea.hy.926 cell line pSport 1 LP016 HINA Adenocarcinoma Human pSport 1 LP016 HRMA Lung Mesothelium pSport 1 LP016 HLCL Human Pre-Differentiated Uni-Zap XR LP017 Adipocytes HS2A Saos2 Cells pSport 1 LP020 HS2I Saos2 Cells; Vitamin D3 Treated pSport 1 LP020 HUCM CHME Cell Line, untreated pSport 1 LP020 HEPN Aryepiglottis Normal pSport 1 LP020 HPSN Sinus Piniformis Tumour pSport 1 LP020 HNSA Stomach Normal pSport 1 LP020 HNSM Stomach Tumour pSport 1 LP020 HNLA Liver Normal Met5No pSport 1 LP020 HUTA Liver Tumour Met 5 Tu pSport 1 LP020 HOCN Colon Normal pSport 1 LP020 HOCT Colon Tumor pSport 1 LP020 HTNT Tongue Tumour pSport 1 LP020 HLXN Larynx Normal pSport 1 LP020 HLXT Larynx Tumour pSport 1 LP020 HTYN Thymus pSport 1 LP020 HPLN Placenta pSport 1 LP020 HTNG Tongue Normal pSport 1 LP020 HZAA Thyroid Normal (SDCA2 No) pSport 1 LP020 HWES Thyroid Thyroiditis pSport 1 LP020 HFHD FICOLL ™ ed Human Stromal pTrip1Ex2 LP021 Cells, 5Fu treated HFHM, HFHN FICOLL ™ ed Human Stromal pTrip1Ex2 LP021 Cells, Untreated HPCI Hep G2 Cells, lambda library lambda Zap-CMV LP021 XR HBCA, HBCB, HBCC H. Lymph node breast Cancer Uni-ZAP XR LP021 HCOK Chondrocytes pSPORT 1 LP022 HDCA, HDCB, HDCC Dendritic Cells From CD34 pSPORT 1 LP022 Cells HDMA, HDMB CD40 activated monocyte pSPORT 1 LP022 dendritic cells HDDM, HDDN, HDDO LPS activated derived dendritic pSPORT 1 LP022 cells HPCR Hep G2 Cells, PCR library lambda Zap-CMV LP022 XR HAAA, HAAB, HAAC Lung, Cancer (4005313A3): pSPORT 1 LP022 Invasive Poorly Differentiated Lung Adenocarcinoma HIPA, HIPB, HIPC Lung, Cancer (4005163 B7): pSPORT 1 LP022 Invasive, Poorly Diff. Adenocarcinoma, Metastatic HOOH, HOOI Ovary, Cancer: (4004562 B6) pSPORT 1 LP022 Papillary Serous Cystic Neoplasm, Low Malignant Pot HIDA Lung, Normal: (4005313 B1) pSPORT 1 LP022 HUJA, HUJB, HUJC, HUJD, HUJE B-Cells pCMVSport 3.0 LP022 HNOA, HNOB, HNOC, HNOD Ovary, Normal: (9805C040R) pSPORT 1 LP022 HNLM Lung, Normal: (4005313 B1) pSPORT 1 LP022 HSCL Stromal Cells pSPORT 1 LP022 HAAX Lung, Cancer: (4005313 A3) pSPORT 1 LP022 Invasive Poorly-differentiated Metastatic lung adenocarcinoma HUUA, HUUB, HUUC, HUUD B-cells (unstimulated) pTrip1Ex2 LP022 HWWA, HWWB, HWWC, HWWD, B-cells (stimulated) pSPORT 1 LP022 HWWE, HWWF, HWWG HCCC Colon, Cancer: (9808C064R) pCMVSport 3.0 LP023 HPDO HPDP HPDQ HPDR Ovary, Cancer (9809C332): pSport 1 LP023 HPD Poorly differentiated adenocarcinoma HPCO HPCP HPCQ HPCT Ovary, Cancer (15395A1F): pSport 1 LP023 Grade II Papillary Carcinoma HOCM HOCO HOCP HOCQ Ovary, Cancer: (15799A1F) pSport 1 LP023 Poorly differentiated carcinoma HCBM HCBN HCBO Breast, Cancer: (4004943 A5) pSport 1 LP023 HNBT HNBU HNBV Breast, Normal: (4005522B2) pSport 1 LP023 HBCP HBCQ Breast, Cancer: (4005522 A2) pSport 1 LP023 HBCJ Breast, Cancer: (9806C012R) pSport 1 LP023 HSAM HSAN Stromal cells 3.88 pSport 1 LP023 HVCA HVCB HVCC HVCD Ovary, Cancer: (4004332 A2) pSport 1 LP023 HSCK HSEN HSEO Stromal cells (HBM3.18) pSport 1 LP023 HSCP HSCQ stromal cell clone 2.5 pSport 1 LP023 HUXA Breast Cancer: (4005385 A2) pSport 1 LP023 HCOM HCON HCOO HCOP Ovary, Cancer (4004650 A3): pSport 1 LP023 HCOQ Well-Differentiated Micropapillary Serous Carcinoma HBNM Breast, Cancer: (9802C020E) pSport 1 LP023 HVVA HVVB HVVC HVVD Human Bone Marrow, treated pSport 1 LP023 HVVE

Two nonlimiting examples are provided below for isolating a particular clone from the deposited sample of plasmid cDNAs cited for that clone in Table 7. First, a plasmid is directly isolated by screening the clones using a polynucleotide probe corresponding to the nucleotide sequence of SEQ ID NO:X.

Particularly, a specific polynucleotide with 30-40 nucleotides is synthesized using an Applied Biosystems DNA synthesizer according to the sequence reported. The oligonucleotide is labeled, for instance, with ³²P-γ-ATP using T4 polynucleotide kinase and purified according to routine methods. (E.g., Maniatis et al., Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Press, Cold Spring, N.Y. (1982)). The plasmid mixture is transformed into a suitable host, as indicated above (such as XL-1 Blue (STRATAGENE™)) using techniques known to those of skill in the art, such as those provided by the vector supplier or in related publications or patents cited above. The transformants are plated on 1.5% agar plates (containing the appropriate selection agent, e.g., ampicillin) to a density of about 150 transformants (colonies) per plate. These plates are screened using Nylon membranes according to routine methods for bacterial colony screening (e.g., Sambrook et al., Molecular Cloning: A Laboratory Manual, 2nd Edit., (1989), Cold Spring Harbor Laboratory Press, pages 1.93 to 1.104), or other techniques known to those of skill in the art.

Alternatively, two primers of 17-20 nucleotides derived from both ends of the nucleotide sequence of SEQ ID NO:X are synthesized and used to amplify the desired cDNA using the deposited cDNA plasmid as a template. The polymerase chain reaction is carried out under routine conditions, for instance, in 25 μl of reaction mixture with 0.5 ug of the above cDNA template. A convenient reaction mixture is 1.5-5 mM MgCl₂, 0.01% (w/v) gelatin, 20 μM each of dATP, dCTP, dGTP, dTTP, 25 μmol of each primer and 0.25 Unit of Taq polymerase. Thirty five cycles of PCR (denaturation at 94° C. for 1 min; annealing at 55° C. for 1 min; elongation at 72° C. for 1 min) are performed with a Perkin-Elmer Cetus automated thermal cycler. The amplified product is analyzed by agarose gel electrophoresis and the DNA band with expected molecular weight is excised and purified. The PCR product is verified to be the selected sequence by subcloning and sequencing the DNA product.

Several methods are available for the identification of the 5′ or 3′ non-coding portions of a gene which may not be present in the deposited clone. These methods include but are not limited to, filter probing, clone enrichment using specific probes, and protocols similar or identical to 5′ and 3′ “RACE” protocols which are well known in the art. For instance, a method similar to 5′ RACE is available for generating the missing 5′ end of a desired full-length transcript. (Fromont-Racine et al., Nucleic Acids Res. 21(7):1683-1684 (1993)).

Briefly, a specific RNA oligonucleotide is ligated to the 5′ ends of a population of RNA presumably containing full-length gene RNA transcripts. A primer set containing a primer specific to the ligated RNA oligonucleotide and a primer specific to a known sequence of the gene of interest is used to PCR amplify the 5′ portion of the desired full-length gene. This amplified product may then be sequenced and used to generate the full length gene.

This above method starts with total RNA isolated from the desired source, although poly-A+ RNA can be used. The RNA preparation can then be treated with phosphatase if necessary to eliminate 5′ phosphate groups on degraded or damaged RNA which may interfere with the later RNA ligase step. The phosphatase should then be inactivated and the RNA treated with tobacco acid pyrophosphatase in order to remove the cap structure present at the 5′ ends of messenger RNAs. This reaction leaves a 5′ phosphate group at the 5′ end of the cap cleaved RNA which can then be ligated to an RNA oligonucleotide using T4 RNA ligase.

This modified RNA preparation is used as a template for first strand cDNA synthesis using a gene specific oligonucleotide. The first strand synthesis reaction is used as a template for PCR amplification of the desired 5′ end using a primer specific to the ligated RNA oligonucleotide and a primer specific to the known sequence of the gene of interest. The resultant product is then sequenced and analyzed to confirm that the 5′ end sequence belongs to the desired gene.

Example 2 Isolation of Genomic Clones Corresponding to a Polynucleotide

A human genomic PI library (Genomic Systems, Inc.) is screened by PCR using primers selected for the sequence corresponding to SEQ ID NO:X according to the method described in Example 1. (See also, Sambrook.)

Example 3 Tissue Specific Expression Analysis

The Human Genome Sciences, Inc. (HGS) database is derived from sequencing tissue and/or disease specific cDNA libraries. Libraries generated from a particular tissue are selected and the specific tissue expression pattern of EST groups or assembled contigs within these libraries is determined by comparison of the expression patterns of those groups or contigs within the entire database. ESTs and assembled contigs which show tissue specific expression are selected.

The original clone from which the specific EST sequence was generated, or in the case of an assembled contig, the clone from which the 5′ most EST sequence was generated, is obtained from the catalogued library of clones and the insert amplified by PCR using methods known in the art. The PCR product is denatured and then transferred in 96 or 384 well format to a nylon membrane (Schleicher and Scheull) generating an array filter of tissue specific clones. Housekeeping genes, maize genes, and known tissue specific genes are included on the filters. These targets can be used in signal normalization and to validate assay sensitivity. Additional targets are included to monitor probe length and specificity of hybridization.

Radioactively labeled hybridization probes are generated by first strand cDNA synthesis per the manufacturer's instructions (LIFE TECHNOLOGIES™) from mRNA/RNA samples prepared from the specific tissue being analyzed (e.g., prostate, prostate cancer, ovarian, ovarian cancer, etc.). The hybridization probes are purified by gel exclusion chromatography, quantitated, and hybridized with the array filters in hybridization bottles at 65° C. overnight. The filters are washed under stringent conditions and signals are captured using a Fuji phosphorimager.

Data is extracted using AIS software and following background subtraction, signal normalization is performed. This includes a normalization of filter-wide expression levels between different experimental runs. Genes that are differentially expressed in the tissue of interest are identified.

Example 4 Chromosomal Mapping of the Polynucleotides

An oligonucleotide primer set is designed according to the sequence at the 5′ end of SEQ ID NO:X. This primer preferably spans about 100 nucleotides. This primer set is then used in a polymerase chain reaction under the following set of conditions: 30 seconds, 95° C.; 1 minute, 56° C.; 1 minute, 70° C. This cycle is repeated 32 times followed by one 5 minute cycle at 70° C. Human, mouse, and hamster DNA is used as template in addition to a somatic cell hybrid panel containing individual chromosomes or chromosome fragments (Bios, Inc). The reactions are analyzed on either 8% polyacrylamide gels or 3.5% agarose gels. Chromosome mapping is determined by the presence of an approximately 100 bp PCR fragment in the particular somatic cell hybrid.

Example 5 Bacterial Expression of a Polypeptide

A polynucleotide encoding a polypeptide of the present invention is amplified using PCR oligonucleotide primers corresponding to the 5′ and 3′ ends of the DNA sequence, as outlined in Example 1, to synthesize insertion fragments. The primers used to amplify the cDNA insert should preferably contain restriction sites, such as BamHI and XbaI, at the 5′ end of the primers in order to clone the amplified product into the expression vector. For example, BamHI and XbaI correspond to the restriction enzyme sites on the bacterial expression vector pQE-9. (Qiagen, Inc., Chatsworth, Calif.). This plasmid vector encodes antibiotic resistance (Amp^(r)), a bacterial origin of replication (ori), an IPTG-regulatable promoter/operator (P/O), a ribosome binding site (RBS), a 6-histidine tag (6-His), and restriction enzyme cloning sites.

The pQE-9 vector is digested with BamHI and XbaI and the amplified fragment is ligated into the pQE-9 vector maintaining the reading frame initiated at the bacterial RBS. The ligation mixture is then used to transform the E. coli strain M15/rep4 (Qiagen, Inc.) which contains multiple copies of the plasmid pREP4, which expresses the lacd repressor and also confers kanamycin resistance (Kan^(r)). Transformants are identified by their ability to grow on LB plates and ampicillin/kanamycin resistant colonies are selected. Plasmid DNA is isolated and confirmed by restriction analysis.

Clones containing the desired constructs are grown overnight (O/N) in liquid culture in LB media supplemented with both Amp (100 ug/ml) and Kan (25 ug/ml). The O/N culture is used to inoculate a large culture at a ratio of 1:100 to 1:250. The cells are grown to an optical density 600 (O.D.⁶⁰⁰) of between 0.4 and 0.6. IPTG (Isopropyl-B-D-thiogalacto pyranoside) is then added to a final concentration of 1 mM. IPTG induces by inactivating the lacd repressor, clearing the P/0 leading to increased gene expression.

Cells are grown for an extra 3 to 4 hours. Cells are then harvested by centrifugation (20 mins at 6000×g). The cell pellet is solubilized in the chaotropic agent 6 Molar Guanidine HCl by stirring for 3-4 hours at 4° C. The cell debris is removed by centrifugation, and the supernatant containing the polypeptide is loaded onto a nickel-nitrilo-tri-acetic acid (“Ni-NTA”) affinity resin column (available from QIAGEN, Inc., supra). Proteins with a 6×His tag bind to the Ni-NTA resin with high affinity and can be purified in a simple one-step procedure (for details see: The QIAexpressionist (1995) QIAGEN, Inc., supra).

Briefly, the supernatant is loaded onto the column in 6 M guanidine-HCl, pH 8. The column is first washed with 10 volumes of 6 M guanidine-HCl, pH 8, then washed with 10 volumes of 6 M guanidine-HCl pH 6, and finally the polypeptide is eluted with 6 M guanidine-HCl, pH 5.

The purified protein is then renatured by dialyzing it against phosphate-buffered saline (PBS) or 50 mM Na-acetate, pH 6 buffer plus 200 mM NaCl. Alternatively, the protein can be successfully refolded while immobilized on the Ni-NTA column. The recommended conditions are as follows: renature using a linear 6M-1M urea gradient in 500 mM NaCl, 20% glycerol, 20 mM Tris/HCl pH 7.4, containing protease inhibitors. The renaturation should be performed over a period of 1.5 hours or more. After renaturation the proteins are eluted by the addition of 250 mM immidazole. Immidazole is removed by a final dialyzing step against PBS or 50 mM sodium acetate pH 6 buffer plus 200 mM NaCl. The purified protein is stored at 4° C. or frozen at −80° C.

In addition to the above expression vector, the present invention further includes an expression vector, called pHE4a (ATCC™ Accession Number 209645, deposited on Feb. 25, 1998) which contains phage operator and promoter elements operatively linked to a polynucleotide of the present invention, called pHE4a. (ATCC™ Accession Number 209645, deposited on Feb. 25, 1998.) This vector contains: 1) a neomycinphosphotransferase gene as a selection marker, 2) an E. coli origin of replication, 3) a T5 phage promoter sequence, 4) two lac operator sequences, 5) a Shine-Delgarno sequence, and 6) the lactose operon repressor gene (lacIq). The origin of replication (oriC) is derived from pUC19 (LTI, Gaithersburg, Md.). The promoter and operator sequences are made synthetically.

DNA can be inserted into the pHE4a by restricting the vector with NdeI and XbaI, BamHI, XhoI, or Asp718, running the restricted product on a gel, and isolating the larger fragment (the stuffer fragment should be about 310 base pairs). The DNA insert is generated according to the PCR protocol described in Example 1, using PCR primers having restriction sites for NdeI (5′ primer) and XbaI, BamHI, XhoI, or Asp718 (3′ primer). The PCR insert is gel purified and restricted with compatible enzymes. The insert and vector are ligated according to standard protocols.

The engineered vector could easily be substituted in the above protocol to express protein in a bacterial system.

Example 6 Purification of a Polypeptide from an Inclusion Body

The following alternative method can be used to purify a polypeptide expressed in E. coli when it is present in the form of inclusion bodies. Unless otherwise specified, all of the following steps are conducted at 4-10° C.

Upon completion of the production phase of the E. coli fermentation, the cell culture is cooled to 4-10C and the cells harvested by continuous centrifugation at 15,000 rpm (Heraeus Sepatech). On the basis of the expected yield of protein per unit weight of cell paste and the amount of purified protein required, an appropriate amount of cell paste, by weight, is suspended in a buffer solution containing 100 mM Tris, 50 mM EDTA, pH 7.4. The cells are dispersed to a homogeneous suspension using a high shear mixer.

The cells are then lysed by passing the solution through a microfluidizer (Microfluidics, Corp. or APV Gaulin, Inc.) twice at 4000-6000 psi. The homogenate is then mixed with NaCl solution to a final concentration of 0.5 M NaCl, followed by centrifugation at 7000×g for 15 min. The resultant pellet is washed again using 0.5M NaCl, 100 mM Tris, 50 mM EDTA, pH 7.4.

The resulting washed inclusion bodies are solubilized with 1.5 M guanidine hydrochloride (GuHCl) for 2-4 hours. After 7000×g centrifugation for 15 min., the pellet is discarded and the polypeptide containing supernatant is incubated at 4° C. overnight to allow further GuHCl extraction.

Following high speed centrifugation (30,000×g) to remove insoluble particles, the GuHCl solubilized protein is refolded by quickly mixing the GuHCl extract with 20 volumes of buffer containing 50 mM sodium, pH 4.5, 150 mM NaCl, 2 mM EDTA by vigorous stirring. The refolded diluted protein solution is kept at 4° C. without mixing for 12 hours prior to further purification steps.

To clarify the refolded polypeptide solution, a previously prepared tangential filtration unit equipped with 0.16 μm membrane filter with appropriate surface area (e.g., Filtron), equilibrated with 40 mM sodium acetate, pH 6.0 is employed. The filtered sample is loaded onto a cation exchange resin (e.g., Poros HS-50, Perseptive Biosystems). The column is washed with 40 mM sodium acetate, pH 6.0 and eluted with 250 mM, 500 mM, 1000 mM, and 1500 mM NaCl in the same buffer, in a stepwise manner. The absorbance at 280 nm of the effluent is continuously monitored. Fractions are collected and further analyzed by SDS-PAGE.

Fractions containing the polypeptide are then pooled and mixed with 4 volumes of water. The diluted sample is then loaded onto a previously prepared set of tandem columns of strong anion (Poros HQ-50, Perseptive Biosystems) and weak anion (Poros CM-20, Perseptive Biosystems) exchange resins. The columns are equilibrated with 40 mM sodium acetate, pH 6.0. Both columns are washed with 40 mM sodium acetate, pH 6.0, 200 mM NaCl. The CM-20 column is then eluted using a 10 column volume linear gradient ranging from 0.2 M NaCl, 50 mM sodium acetate, pH 6.0 to 1.0 M NaCl, 50 mM sodium acetate, pH 6.5. Fractions are collected under constant A₂₈₀ monitoring of the effluent. Fractions containing the polypeptide (determined, for instance, by 16% SDS-PAGE) are then pooled.

The resultant polypeptide should exhibit greater than 95% purity after the above refolding and purification steps. No major contaminant bands should be observed from Commassie blue stained 16% SDS-PAGE gel when 5 μg of purified protein is loaded. The purified protein can also be tested for endotoxin/LPS contamination, and typically the LPS content is less than 0.1 ng/ml according to LAL assays.

Example 7 Cloning and Expression of a Polypeptide in a Baculovirus Expression System

In this example, the plasmid shuttle vector pA2 is used to insert a polynucleotide into a baculovirus to express a polypeptide. This expression vector contains the strong polyhedrin promoter of the Autographa californica nuclear polyhedrosis virus (AcMNPV) followed by convenient restriction sites such as BamHI, Xba I and Asp718. The polyadenylation site of the simian virus 40 (“SV40”) is used for efficient polyadenylation. For easy selection of recombinant virus, the plasmid contains the beta-galactosidase gene from E. coli under control of a weak Drosophila promoter in the same orientation, followed by the polyadenylation signal of the polyhedrin gene. The inserted genes are flanked on both sides by viral sequences for cell-mediated homologous recombination with wild-type viral DNA to generate a viable virus that express the cloned polynucleotide.

Many other baculovirus vectors can be used in place of the vector above, such as pAc373, pVL941, and pAcIM1, as one skilled in the art would readily appreciate, as long as the construct provides appropriately located signals for transcription, translation, secretion and the like, including a signal peptide and an in-frame AUG as required. Such vectors are described, for instance, in Luckow et al., Virology 170:31-39 (1989).

Specifically, the cDNA sequence contained in the deposited clone, including the AUG initiation codon, is amplified using the PCR protocol described in Example 1. If a naturally occurring signal sequence is used to produce the polypeptide of the present invention, the pA2 vector does not need a second signal peptide. Alternatively, the vector can be modified (pA2 GP) to include a baculovirus leader sequence, using the standard methods described in Summers et al., “A Manual of Methods for Baculovirus Vectors and Insect Cell Culture Procedures,” Texas Agricultural Experimental Station Bulletin No. 1555 (1987).

The amplified fragment is isolated from a 1% agarose gel using a commercially available kit (“GENECLEAN™,” BIO 101 Inc., La Jolla, Calif.). The fragment then is digested with appropriate restriction enzymes and again purified on a 1% agarose gel.

The plasmid is digested with the corresponding restriction enzymes and optionally, can be dephosphorylated using calf intestinal phosphatase, using routine procedures known in the art. The DNA is then isolated from a 1% agarose gel using a commercially available kit (“GENECLEAN™” BIO 101 Inc., La Jolla, Calif.).

The fragment and the dephosphorylated plasmid are ligated together with T4 DNA ligase. E. coli HB101 or other suitable E. coli hosts such as XL-1 Blue (STRATAGENE™ Cloning Systems, La Jolla, Calif.) cells are transformed with the ligation mixture and spread on culture plates. Bacteria containing the plasmid are identified by digesting DNA from individual colonies and analyzing the digestion product by gel electrophoresis. The sequence of the cloned fragment is confirmed by DNA sequencing.

Five μg of a plasmid containing the polynucleotide is co-transfected with 1.0 μg of a commercially available linearized baculovirus DNA (“BACULOGOLD™ baculovirus DNA, Pharmingen, San Diego, Calif.), using the lipofection method described by Felgner et al., Proc. Natl. Acad. Sci. USA 84:7413-7417 (1987). One μg of BACULOGOLD™ virus DNA and 5 μg of the plasmid are mixed in a sterile well of a microtiter plate containing 50 μl of serum-free Grace's medium (LIFE TECHNOLOGIES™ Inc., Gaithersburg, Md.). Afterwards, 10 μl LIPOFECTIN™ plus 90 μl Grace's medium are added, mixed and incubated for 15 minutes at room temperature. Then the transfection mixture is added drop-wise to Sf9 insect cells (ATCC™ CRL 1711) seeded in a 35 mm tissue culture plate with 1 ml Grace's medium without serum. The plate is then incubated for 5 hours at 27° C. The transfection solution is then removed from the plate and 1 ml of Grace's insect medium supplemented with 10% fetal calf serum is added. Cultivation is then continued at 27° C. for four days.

After four days the supernatant is collected and a plaque assay is performed, as described by Summers and Smith, supra. An agarose gel with “Blue Gal” (LIFE TECHNOLOGIES™Inc., Gaithersburg) is used to allow easy identification and isolation of gal-expressing clones, which produce blue-stained plaques. (A detailed description of a “plaque assay” of this type can also be found in the user's guide for insect cell culture and baculovirology distributed by LIFE TECHNOLOGIES™ Inc., Gaithersburg, page 9-10.) After appropriate incubation, blue stained plaques are picked with the tip of a micropipettor (e.g., Eppendorf). The agar containing the recombinant viruses is then resuspended in a microcentrifuge tube containing 200 μl of Grace's medium and the suspension containing the recombinant baculovirus is used to infect Sf9 cells seeded in 35 mm dishes. Four days later the supernatants of these culture dishes are harvested and then they are stored at 4° C.

To verify the expression of the polypeptide, Sf9 cells are grown in Grace's medium supplemented with 10% heat-inactivated FBS. The cells are infected with the recombinant baculovirus containing the polynucleotide at a multiplicity of infection (“MOI”) of about 2. If radiolabeled proteins are desired, 6 hours later the medium is removed and is replaced with SF900 II medium minus methionine and cysteine (available from LIFE TECHNOLOGIES™ Inc., Rockville, Md.). After 42 hours, 5 μCi of ³⁵S-methionine and 5 μCi ³⁵S-cysteine (available from Amersham) are added. The cells are further incubated for 16 hours and then are harvested by centrifugation. The proteins in the supernatant as well as the intracellular proteins are analyzed by SDS-PAGE followed by autoradiography (if radiolabeled).

Microsequencing of the amino acid sequence of the amino terminus of purified protein may be used to determine the amino terminal sequence of the produced protein.

Example 8 Expression of a Polypeptide in Mammalian Cells

The polypeptide of the present invention can be expressed in a mammalian cell. A typical mammalian expression vector contains a promoter element, which mediates the initiation of transcription of mRNA, a protein coding sequence, and signals required for the termination of transcription and polyadenylation of the transcript. Additional elements include enhancers, Kozak sequences and intervening sequences flanked by donor and acceptor sites for RNA splicing. Highly efficient transcription is achieved with the early and late promoters from SV40, the long terminal repeats (LTRs) from Retroviruses, e.g., RSV, HTLVI, HIVI and the early promoter of the cytomegalovirus (CMV). However, cellular elements can also be used (e.g., the human actin promoter).

Suitable expression vectors for use in practicing the present invention include, for example, vectors such as pSVL and pMSG (PHARMACIA™, Uppsala, Sweden), pRSVcat (ATCC™ 37152), pSV2dhfr (ATCC™ 37146), pBC12MI (ATCC™ 67109), pCMVSport 2.0, and pCMVSport 3.0. Mammalian host cells that could be used include, human Hela, 293, H9 and Jurkat cells, mouse NIH3T3 and C127 cells, Cos 1, Cos 7 and CV1, quail QC1-3 cells, mouse L cells and Chinese hamster ovary (CHO) cells.

Alternatively, the polypeptide can be expressed in stable cell lines containing the polynucleotide integrated into a chromosome. The co-transfection with a selectable marker such as DHFR, gpt, neomycin, or hygromycin allows the identification and isolation of the transfected cells.

The transfected gene can also be amplified to express large amounts of the encoded protein. The DHFR (dihydrofolate reductase) marker is useful in developing cell lines that carry several hundred or even several thousand copies of the gene of interest. (See, e.g., Alt, F. W., et al., J. Biol. Chem. 253:1357-1370 (1978); Hamlin, J. L. and Ma, C., Biochem. et Biophys. Acta, 1097:107-143 (1990); Page, M. J. and Sydenham, M. A., Biotechnology 9:64-68 (1991)). Another useful selection marker is the enzyme glutamine synthase (GS) (Murphy et al., Biochem J. 227:277-279 (1991); Bebbington et al., Bio/Technology 10:169-175 (1992). Using these markers, the mammalian cells are grown in selective medium and the cells with the highest resistance are selected. These cell lines contain the amplified gene(s) integrated into a chromosome. Chinese hamster ovary (CHO) and NSO cells are often used for the production of proteins.

Derivatives of the plasmid pSV2-dhfr (ATCC™ Accession No. 37146), the expression vectors pC4 (ATCC™ Accession No. 209646) and pC6 (ATCC™ Accession No. 209647) contain the strong promoter (LTR) of the Rous Sarcoma Virus (Cullen et al., Molecular and Cellular Biology, 438-447 (March, 1985)) plus a fragment of the CMV-enhancer (Boshart et al., Cell 41:521-530 (1985)). Multiple cloning sites, e.g., with the restriction enzyme cleavage sites BamHI, XbaI and Asp718, facilitate the cloning of the gene of interest. The vectors also contain the 3′ intron, the polyadenylation and termination signal of the rat preproinsulin gene, and the mouse DHFR gene under control of the SV40 early promoter.

Specifically, the plasmid pC6, for example, is digested with appropriate restriction enzymes and then dephosphorylated using calf intestinal phosphates by procedures known in the art. The vector is then isolated from a 1% agarose gel.

A polynucleotide of the present invention is amplified according to the protocol outlined in Example 1. If a naturally occurring signal sequence is used to produce the polypeptide of the present invention, the vector does not need a second signal peptide. Alternatively, if a naturally occurring signal sequence is not used, the vector can be modified to include a heterologous signal sequence. (See, e.g., International Publication No. WO 96/34891.)

The amplified fragment is isolated from a 1% agarose gel using a commercially available kit (“GENECLEAN™,” BIO 101 Inc., La Jolla, Calif.). The fragment then is digested with appropriate restriction enzymes and again purified on a 1% agarose gel.

The amplified fragment is then digested with the same restriction enzyme and purified on a 1% agarose gel. The isolated fragment and the dephosphorylated vector are then ligated with T4 DNA ligase. E. coli HB101 or XL-1 Blue cells are then transformed and bacteria are identified that contain the fragment inserted into plasmid pC6 using, for instance, restriction enzyme analysis.

Chinese hamster ovary cells lacking an active DHFR gene is used for transfection. Five μg of the expression plasmid pC6 or pC4 is cotransfected with 0.5 μg of the plasmid pSVneo using LIPOFECTIN™ (Felgner et al., supra). The plasmid pSV2-neo contains a dominant selectable marker, the neo gene from Tn5 encoding an enzyme that confers resistance to a group of antibiotics including G418. The cells are seeded in alpha minus MEM supplemented with 1 mg/ml G418. After 2 days, the cells are trypsinized and seeded in hybridoma cloning plates (Greiner, Germany) in alpha minus MEM supplemented with 10, 25, or 50 ng/ml of methotrexate plus 1 mg/ml G418. After about 10-14 days single clones are trypsinized and then seeded in 6-well petri dishes or 10 ml flasks using different concentrations of methotrexate (50 nM, 100 nM, 200 nM, 400 nM, 800 nM). Clones growing at the highest concentrations of methotrexate are then transferred to new 6-well plates containing even higher concentrations of methotrexate (1 μM, 2 μM, 5 μM, 10 mM, 20 mM). The same procedure is repeated until clones are obtained which grow at a concentration of 100-200 μM. Expression of the desired gene product is analyzed, for instance, by SDS-PAGE and Western blot or by reversed phase HPLC analysis.

Example 9 Protein Fusions

The polypeptides of the present invention are preferably fused to other proteins. These fusion proteins can be used for a variety of applications. For example, fusion of the present polypeptides to His-tag, HA-tag, protein A, IgG domains, and maltose binding protein facilitates purification. (See Example 5; see also EP A 394,827; Traunecker, et al., Nature 331:84-86 (1988)). Similarly, fusion to IgG-1, IgG-3, and albumin increases the halflife time in vivo. Nuclear localization signals fused to the polypeptides of the present invention can target the protein to a specific subcellular localization, while covalent heterodimer or homodimers can increase or decrease the activity of a fusion protein. Fusion proteins can also create chimeric molecules having more than one function. Finally, fusion proteins can increase solubility and/or stability of the fused protein compared to the non-fused protein. All of the types of fusion proteins described above can be made by modifying the following protocol, which outlines the fusion of a polypeptide to an IgG molecule, or the protocol described in Example 5.

Briefly, the human Fc portion of the IgG molecule can be PCR amplified, using primers that span the 5′ and 3′ ends of the sequence described below. These primers also should have convenient restriction enzyme sites that will facilitate cloning into an expression vector, preferably a mammalian expression vector.

For example, if pC4 (ATCC™ Accession No. 209646) is used, the human Fc portion can be ligated into the BamHI cloning site. Note that the 3′ BamHI site should be destroyed. Next, the vector containing the human Fc portion is re-restricted with BamHI, linearizing the vector, and a polynucleotide of the present invention, isolated by the PCR protocol described in Example 1, is ligated into this BamHI site. Note that the polynucleotide is cloned without a stop codon, otherwise a fusion protein will not be produced.

If the naturally occurring signal sequence is used to produce the polypeptide of the present invention, pC4 does not need a second signal peptide. Alternatively, if the naturally occurring signal sequence is not used, the vector can be modified to include a heterologous signal sequence. (See, e.g., International Publication No. WO 96/34891.)

Human IgG Fc region: (SEQ ID NO:1) GGGATCCGGAGCCCAAATCTTCTGACAAAACTCACACATGCCCACCGTGC CCAGCACCTGAATTCGAGGGTGCACCGTCAGTCTTCCTCTTCCCCCCAAA ACCCAAGGACACCCTCATGATCTCCCGGACTCCTGAGGTCACATGCGTGG TGGTGGACGTAAGCCACGAAGACCCTGAGGTCAAGTTCAACTGGTACGTG GACGGCGTGGAGGTGCATAATGCCAAGACAAAGCCGCGGGAGGAGCAGTA CAACAGCACGTACCGTGTGGTCAGCGTCCTCACCGTCCTGCACCAGGACT GGCTGAATGGCAAGGAGTACAAGTGCAAGGTCTCCAACAAAGCCCTCCCA ACCCCCATCGAGAAAACCATCTCCAAAGCCAAAGGGCAGCCCCGAGAACC ACAGGTGTACACCCTGCCCCCATCCCGGGATGAGCTGACCAAGAACCAGG TCAGCCTGACCTGCCTGGTCAAAGGCTTCTATCCAAGCGACATCGCCGTG GAGTGGGAGAGCAATGGGCAGCCGGAGAACAACTACAAGACCACGCCTCC CGTGCTGGACTCCGACGGCTCCTTCTTCCTCTACAGCAAGCTCACCGTGG ACAAGAGCAGGTGGCAGCAGGGGAACGTCTTCTCATGCTCCGTGATGCAT GAGGCTCTGCACAACCACTACACGCAGAAGAGCCTCTCCCTGTCTCCGGG TAAATGAGTGCGACGGCCGCGACTCTAGAGGAT

Example 10 Production of an Antibody from a Polypeptide

a) Hybridoma Technology

The antibodies of the present invention can be prepared by a variety of methods. (See, Current Protocols, Chapter 2.) As one example of such methods, cells expressing a polypeptide of the present invention are administered to an animal to induce the production of sera containing polyclonal antibodies. In a preferred method, a preparation of a polypeptide of the present invention is prepared and purified to render it substantially free of natural contaminants. Such a preparation is then introduced into an animal in order to produce polyclonal antisera of greater specific activity.

Monoclonal antibodies specific for a polypeptide of the present invention are prepared using hybridoma technology (Kohler et al., Nature 256:495 (1975); Kohler et al., Eur. J. Immunol. 6:511 (1976); Kohler et al., Eur. J. Immunol. 6:292 (1976); Hammerling et al., in: Monoclonal Antibodies and T-Cell Hybridomas, Elsevier, N.Y., pp. 563-681 (1981)). In general, an animal (preferably a mouse) is immunized with a polypeptide of the present invention or, more preferably, with a secreted polypeptide-expressing cell. Such polypeptide-expressing cells are cultured in any suitable tissue culture medium, preferably in Earle's modified Eagle's medium supplemented with 10% fetal bovine serum (inactivated at about 56° C.), and supplemented with about 10 g/l of nonessential amino acids, about 1,000 U/ml of penicillin, and about 100 μg/ml of streptomycin.

The splenocytes of such mice are extracted and fused with a suitable myeloma cell line. Any suitable myeloma cell line may be employed in accordance with the present invention; however, it is preferable to employ the parent myeloma cell line (SP20), available from the ATCC™. After fusion, the resulting hybridoma cells are selectively maintained in HAT medium, and then cloned by limiting dilution as described by Wands et al. (Gastroenterology 80:225-232 (1981)). The hybridoma cells obtained through such a selection are then assayed to identify clones which secrete antibodies capable of binding the polypeptide of the present invention.

Alternatively, additional antibodies capable of binding to a polypeptide of the present invention can be produced in a two-step procedure using anti-idiotypic antibodies. Such a method makes use of the fact that antibodies are themselves antigens, and therefore, it is possible to obtain an antibody which binds to a second antibody. In accordance with this method, protein specific antibodies are used to immunize an animal, preferably a mouse. The splenocytes of such an animal are then used to produce hybridoma cells, and the hybridoma cells are screened to identify clones which produce an antibody whose ability to bind to the polypeptide-specific antibody can be blocked by said polypeptide. Such antibodies comprise anti-idiotypic antibodies to the polypeptide-specific antibody and are used to immunize an animal to induce formation of further polypeptide-specific antibodies.

For in vivo use of antibodies in humans, an antibody is “humanized”. Such antibodies can be produced using genetic constructs derived from hybridoma cells producing the monoclonal antibodies described above. Methods for producing chimeric and humanized antibodies are known in the art and are discussed herein. (See, for review, Morrison, Science 229:1202 (1985); Oi et al., BioTechniques 4:214 (1986); Cabilly et al., U.S. Pat. No. 4,816,567; Taniguchi et al., EP 171496; Morrison et al., EP 173494; Neuberger et al., WO 8601533; Robinson et al., International Publication No. WO 8702671; Boulianne et al., Nature 312:643 (1984); Neuberger et al., Nature 314:268 (1985)).

b) Isolation of Antibody Fragments Directed Against a Polypeptide of the Present Invention from a Library of scFvs

Naturally occurring V-genes isolated from human PBLs are constructed into a library of antibody fragments which contain reactivities against a polypeptide of the present invention to which the donor may or may not have been exposed (see e.g., U.S. Pat. No. 5,885,793 incorporated herein by reference in its entirety).

Rescue of the Library. A library of scFvs is constructed from the RNA of human PBLs as described in International Publication No. WO 92/01047. To rescue phage displaying antibody fragments, approximately 10⁹ E. coli harboring the phagemid are used to inoculate 50 ml of 2×TY containing 1% glucose and 100 μg/ml of ampicillin (2×TY-AMP-GLU) and grown to an O.D. of 0.8 with shaking. Five ml of this culture is used to inoculate 50 ml of 2×TY-AMP-GLU, 2×108 TU of delta gene 3 helper (M13 delta gene III, see International Publication No. WO 92/01047) are added and the culture incubated at 37° C. for 45 minutes without shaking and then at 37° C. for 45 minutes with shaking. The culture is centrifuged at 4000 r.p.m. for 10 min. and the pellet resuspended in 2 liters of 2xTY containing 100 μg/ml ampicillin and 50 ug/ml kanamycin and grown overnight. Phage are prepared as described in International Publication No. WO 92/01047.

M13 delta gene III is prepared as follows: M13 delta gene III helper phage does not encode gene III protein, hence the phage (mid) displaying antibody fragments have a greater avidity of binding to antigen. Infectious M13 delta gene III particles are made by growing the helper phage in cells harboring a pUC19 derivative supplying the wild type gene III protein during phage morphogenesis. The culture is incubated for 1 hour at 37° C. without shaking and then for a further hour at 37° C. with shaking. Cells are spun down (IEC-Centra 8,400 r.p.m. for 10 min), resuspended in 300 ml 2xTY broth containing 100 μg ampicillin/ml and 25 μg kanamycin/ml (2xTY-AMP-KAN) and grown overnight, shaking at 37° C. Phage particles are purified and concentrated from the culture medium by two PEG-precipitations (Sambrook et al., 1990), resuspended in 2 ml PBS and passed through a 0.45 μm filter (Minisart NML; Sartorius) to give a final concentration of approximately 10¹³ transducing units/ml (ampicillin-resistant clones).

Panning of the Library. Immunotubes (Nunc) are coated overnight in PBS with 4 ml of either 100 μg/ml or 10 μg/ml of a polypeptide of the present invention. Tubes are blocked with 2% Marvel-PBS for 2 hours at 37° C. and then washed 3 times in PBS. Approximately 10¹³ TU of phage is applied to the tube and incubated for 30 minutes at room temperature tumbling on an over and under turntable and then left to stand for another 1.5 hours. Tubes are washed 10 times with PBS 0.1% Tween-20 and 10 times with PBS. Phage are eluted by adding 1 ml of 100 mM triethylamine and rotating 15 minutes on an under and over turntable after which the solution is immediately neutralized with 0.5 ml of 1.0M Tris-HCl, pH 7.4. Phage are then used to infect 10 ml of mid-log E. coli TG1 by incubating eluted phage with bacteria for 30 minutes at 37° C. The E. coli are then plated on TYE plates containing 1% glucose and 100 μg/ml ampicillin. The resulting bacterial library is then rescued with delta gene 3 helper phage as described above to prepare phage for a subsequent round of selection. This process is then repeated for a total of 4 rounds of affinity purification with tube-washing increased to 20 times with PBS, 0.1% Tween-20 and 20 times with PBS for rounds 3 and 4.

Characterization of Binders. Eluted phage from the 3rd and 4th rounds of selection are used to infect E. coli HB 2151 and soluble scFv is produced (Marks, et al., 1991) from single colonies for assay. ELISAs are performed with microtitre plates coated with either 10 pg/ml of the polypeptide of the present invention in 50 mM bicarbonate pH 9.6. Clones positive in ELISA are further characterized by PCR fingerprinting (see, e.g., International Publication No. WO 92/01047) and then by sequencing. These ELISA positive clones may also be further characterized by techniques known in the art, such as, for example, epitope mapping, binding affinity, receptor signal transduction, ability to block or competitively inhibit antibody/antigen binding, and competitive agonistic or antagonistic activity.

Example 11 Method of Determining Alterations in a Gene Corresponding to a Polynucleotide

RNA isolated from entire families or individual patients presenting with cancer or a hyperproliferative disease or disorder is isolated. cDNA is then generated from these RNA samples using protocols known in the art. (See, Sambrook.) The cDNA is then used as a template for PCR, employing primers surrounding regions of interest in SEQ ID NO:X; and/or the nucleotide sequence of the cDNA contained in ATCC™ Deposit No:Z. Suggested PCR conditions consist of 35 cycles at 95 degrees C. for 30 seconds; 60-120 seconds at 52-58 degrees C.; and 60-120 seconds at 70 degrees C., using buffer solutions described in Sidransky et al., Science 252:706 (1991).

PCR products are then sequenced using primers labeled at their 5′ end with T4 polynucleotide kinase, employing SequiTherm Polymerase (Epicentre Technologies). The intron-exon boundaries of selected exons is also determined and genomic PCR products analyzed to confirm the results. PCR products harboring suspected mutations are then cloned and sequenced to validate the results of the direct sequencing.

PCR products are cloned into T-tailed vectors as described in Holton et al., Nucleic Acids Research, 19:1156 (1991) and sequenced with T7 polymerase (United States Biochemical). Affected individuals are identified by mutations not present in unaffected individuals.

Genomic rearrangements are also observed as a method of determining alterations in a gene corresponding to a polynucleotide. Genomic clones isolated according to Example 2 are nick-translated with digoxigenindeoxy-uridine 5′-triphosphate (BOEHRINGER™ Manheim), and FISH performed as described in Johnson et al., Methods Cell Biol. 35:73-99 (1991). Hybridization with the labeled probe is carried out using a vast excess of human cot-1 DNA for specific hybridization to the corresponding genomic locus.

Chromosomes are counterstained with 4,6-diamino-2-phenylidole and propidium iodide, producing a combination of C- and R-bands. Aligned images for precise mapping are obtained using a triple-band filter set (Chroma Technology, Brattleboro, Vt.) in combination with a cooled charge-coupled device camera (Photometrics, Tucson, Ariz.) and variable excitation wavelength filters. (Johnson et al., Genet. Anal. Tech. Appl., 8:75 (1991)). Image collection, analysis and chromosomal fractional length measurements are performed using the ISee Graphical Program System. (Inovision Corporation, Durham, N.C.) Chromosome alterations of the genomic region hybridized by the probe are identified as insertions, deletions, and translocations. These alterations are used as a diagnostic marker for an associated disease.

Example 12 Method of Detecting Abnormal Levels of a Polypeptide in a Biological Sample

A polypeptide of the present invention can be detected in a biological sample, and if an increased or decreased level of the polypeptide is detected, this polypeptide is a marker for a particular phenotype. Methods of detection are numerous, and thus, it is understood that one skilled in the art can modify the following assay to fit their particular needs.

For example, antibody-sandwich ELISAs are used to detect polypeptides in a sample, preferably a biological sample. Wells of a microtiter plate are coated with specific antibodies, at a final concentration of 0.2 to 10 ug/ml. The antibodies are either monoclonal or polyclonal and are produced by the method described in Example 10. The wells are blocked so that non-specific binding of the polypeptide to the well is reduced.

The coated wells are then incubated for >2 hours at RT with a sample containing the polypeptide. Preferably, serial dilutions of the sample should be used to validate results. The plates are then washed three times with deionized or distilled water to remove unbound polypeptide.

Next, 50 ul of specific antibody-alkaline phosphatase conjugate, at a concentration of 25-400 ng, is added and incubated for 2 hours at room temperature. The plates are again washed three times with deionized or distilled water to remove unbound conjugate.

Add 75 ul of 4-methylumbelliferyl phosphate (MUP) or p-nitrophenyl phosphate APP) substrate solution to each well and incubate 1 hour at room temperature. Measure the reaction by a microtiter plate reader. Prepare a standard curve, using serial dilutions of a control sample, and plot polypeptide concentration on the X-axis (log scale) and fluorescence or absorbance of the Y-axis (linear scale). Interpolate the concentration of the polypeptide in the sample using the standard curve.

Example 13 Formulation

The invention also provides methods of preventing, treating and/or ameliorating cancer or other hyperproliferative disorders by administration to a subject of an effective amount of a Therapeutic. By therapeutic is meant polynucleotides or polypeptides of the invention (including fragments and variants), agonists or antagonists thereof, and/or antibodies thereto, in combination with a pharmaceutically acceptable carrier type (e.g., a sterile carrier).

The Therapeutic will be formulated and dosed in a fashion consistent with good medical practice, taking into account the clinical condition of the individual patient (especially the side effects of treatment with the Therapeutic alone), the site of delivery, the method of administration, the scheduling of administration, and other factors known to practitioners. The “effective amount” for purposes herein is thus determined by such considerations.

As a general proposition, the total pharmaceutically effective amount of the Therapeutic administered parenterally per dose will be in the range of about 1 ug/kg/day to 10 mg/kg/day of patient body weight, although, as noted above, this will be subject to therapeutic discretion. More preferably, this dose is at least 0.01 mg/kg/day, and most preferably for humans between about 0.01 and 1 mg/kg/day for the hormone. If given continuously, the Therapeutic is typically administered at a dose rate of about 1 ug/kg/hour to about 50 ug/kg/hour, either by 1-4 injections per day or by continuous subcutaneous infusions, for example, using a mini-pump. An intravenous bag solution may also be employed. The length of treatment needed to observe changes and the interval following treatment for responses to occur appears to vary depending on the desired effect.

Therapeutics can be are administered orally, rectally, parenterally, intracistemally, intravaginally, intraperitoneally, topically (as by powders, ointments, gels, drops or transdermal patch), bucally, or as an oral or nasal spray. “Pharmaceutically acceptable carrier” refers to a non-toxic solid, semisolid or liquid filler, diluent, encapsulating material or formulation auxiliary of any. The term “parenteral” as used herein refers to modes of administration which include intravenous, intramuscular, intraperitoneal, intrasternal, subcutaneous and intraarticular injection and infusion.

Therapeutics of the invention are also suitably administered by sustained-release systems. Suitable examples of sustained-release Therapeutics are administered orally, rectally, parenterally, intracistemally, intravaginally, intraperitoneally, topically (as by powders, ointments, gels, drops or transdermal patch), bucally, or as an oral or nasal spray. “Pharmaceutically acceptable carrier” refers to a non-toxic solid, semisolid or liquid filler, diluent, encapsulating material or formulation auxiliary of any type. The term “parenteral” as used herein refers to modes of administration which include intravenous, intramuscular, intraperitoneal, intrasternal, subcutaneous and intraarticular injection and infusion.

Therapeutics of the invention are also suitably administered by sustained-release systems. Suitable examples of sustained-release Therapeutics include suitable polymeric materials (such as, for example, semi-permeable polymer matrices in the form of shaped articles, e.g., films, or mirocapsules), suitable hydrophobic materials (for example as an emulsion in an acceptable oil) or ion exchange resins, and sparingly soluble derivatives (such as, for example, a sparingly soluble salt).

Sustained-release matrices include polylactides (U.S. Pat. No. 3,773,919, EP 58,481), copolymers of L-glutamic acid and gamma-ethyl-L-glutamate (Sidman et al., Biopolymers 22:547-556 (1983)), poly (2-hydroxyethyl methacrylate) (Langer et al., J. Biomed. Mater. Res. 15:167-277 (1981), and Langer, Chem. Tech. 12:98-105 (1982)), ethylene vinyl acetate (Langer et al., Id.) or poly-D-(−)-3-hydroxybutyric acid (EP 133,988).

In a preferred embodiment, polypeptide, polynucleotide, and antibody compositions of the invention are formulated in a biodegradable, polymeric drug delivery system, for example as described in U.S. Pat. Nos. 4,938,763; 5,278,201; 5,278,202; 5,324,519; 5,340,849; and 5,487,897 and in International Publication Numbers WO01/35929, WO00/24374, and WO00/06117 which are hereby incorporated by reference in their entirety. In specific preferred embodiments the polypeptide, polynucleotide, and antibody compositions of the invention are formulated using the ATRIGEL® Biodegradable System of Atrix Laboratories, Inc. (Fort Collins, Colo.).

Examples of biodegradable polymers which can be used in the formulation of polypeptide, polynucleotide, and antibody compositions, include but are not limited to, polylactides, polyglycolides, polycaprolactones, polyanhydrides, polyamides, polyurethanes, polyesteramides, polyorthoesters, polydioxanones, polyacetals, polyketals, polycarbonates, polyorthocarbonates, polyphosphazenes, polyhydroxybutyrates, polyhydroxyvalerates, polyalkylene oxalates, polyalkylene succinates, poly(malic acid), poly(amino acids), poly(methyl vinyl ether), poly(maleic anhydride), polyvinylpyrrolidone, polyethylene glycol, polyhydroxycellulose, chitin, chitosan, and copolymers, terpolymers, or combinations or mixtures of the above materials. The preferred polymers are those that have a lower degree of crystallization and are more hydrophobic. These polymers and copolymers are more soluble in the biocompatible solvents than the highly crystalline polymers such as polyglycolide and chitin which also have a high degree of hydrogen-bonding. Preferred materials with the desired solubility parameters are the polylactides, polycaprolactones, and copolymers of these with glycolide in which there are more amorphous regions to enhance solubility. In specific preferred embodiments, the biodegradable polymers which can be used in the formulation of polypeptide, polynucleotide, and antibody compositions are poly(lactide-co-glycolides). Polymer properties such as molecular weight, hydrophobicity, and lactide/glycolide ratio may be modified to obtain the desired polypeptide, polynucleotide, or antibody release profile (See, e.g., Ravivarapu et al., Journal of Pharmaceutical Sciences 89:732-741 (2000), which is hereby incorporated by reference in its entirety).

It is also preferred that the solvent for the biodegradable polymer be non-toxic, water miscible, and otherwise biocompatible. Examples of such solvents include, but are not limited to, N-methyl-2-pyrrolidone, 2-pyrrolidone, C2 to C6 alkanols, C1 to C15 alchohols, dils, triols, and tetraols such as ethanol, glycerine propylene glycol, butanol; C3 to C15 alkyl ketones such as acetone, diethyl ketone and methyl ethyl ketone; C3 to C15 esters such as methyl acetate, ethyl acetate, ethyl lactate; alkyl ketones such as methyl ethyl ketone, C1 to C15 amides such as dimethylformamide, dimethylacetamide and caprolactam; C3 to C20 ethers such as tetrahydrofuran, or solketal; tweens, triacetin, propylene carbonate, decylmethylsulfoxide, dimethyl sulfoxide, oleic acid, 1-dodecylazacycloheptan-2-one, Other preferred solvents are benzyl alchohol, benzyl benzoate, dipropylene glycol, tributyrin, ethyl oleate, glycerin, glycofural, isopropyl myristate, isopropyl palmitate, oleic acid, polyethylene glycol, propylene carbonate, and triethyl citrate. The most preferred solvents are N-methyl-2-pyrrolidone, 2-pyrrolidone, dimethyl sulfoxide, triacetin, and propylene carbonate because of the solvating ability and their compatibility.

Additionally, formulations comprising polypeptide, polynucleotide, and antibody compositions and a biodegradable polymer may also include release-rate modification agents and/or pore-forming agents. Examples of release-rate modification agents include, but are not limited to, fatty acids, triglycerides, other like hydrophobic compounds, organic solvents, plasticizing compounds and hydrophilic compounds. Suitable release rate modification agents include, for example, esters of mono-, di-, and tricarboxylic acids, such as 2-ethoxyethyl acetate, methyl acetate, ethyl acetate, diethyl phthalate, dimethyl phthalate, dibutyl phthalate, dimethyl adipate, dimethyl succinate, dimethyl oxalate, dimethyl citrate, triethyl citrate, acetyl tributyl citrate, acetyl triethyl citrate, glycerol triacetate, di(n-butyl) sebecate, and the like; polyhydroxy alcohols, such as propylene glycol, polyethylene glycol, glycerin, sorbitol, and the like; fatty acids; triesters of glycerol, such as triglycerides, epoxidized soybean oil, and other epoxidized vegetable oils; sterols, such as cholesterol; alcohols, such as C.sub.6-C.sub. 12 alkanols, 2-ethoxyethanol. The release rate modification agent may be used singly or in combination with other such agents. Suitable combinations of release rate modification agents include, but are not limited to, glycerin/propylene glycol, sorbitol/glycerine, ethylene oxide/propylene oxide, butylene glycol/adipic acid, and the like. Preferred release rate modification agents include, but are not limited to, dimethyl citrate, triethyl citrate, ethyl heptanoate, glycerin, and hexanediol. Suitable pore-forming agents that may be used in the polymer composition include, but are not limited to, sugars such as sucrose and dextrose, salts such as sodium chloride and sodium carbonate, polymers such as hydroxylpropylcellulose, carboxymethylcellulose, polyethylene glycol, and polyvinylpyrrolidone. Solid crystals that will provide a defined pore size, such as salt or sugar, are preferred.

In specific preferred embodiments the polypeptide, polynucleotide, and antibody compositions of the invention are formulated using the BEMA™ BioErodible Mucoadhesive System, MCA™ MucoCutaneous Absorption System, SMP™ Solvent MicroParticle System, or BCP™ BioCompatible Polymer System of Atrix Laboratories, Inc. (Fort Collins, Colo.).

Sustained-release Therapeutics also include liposomally entrapped Therapeutics of the invention (see generally, Langer, Science 249:1527-1533 (1990); Treat et al., in Liposomes in the Therapy of Infectious Disease and Cancer, Lopez-Berestein and Fidler (eds.), Liss, New York, pp. 317-327 and 353-365 (1989)). Liposomes containing the Therapeutic are prepared by methods known per se: DE 3,218,121; Epstein et al., Proc. Natl. Acad. Sci. (USA) 82:3688-3692 (1985); Hwang et al., Proc. Natl. Acad. Sci. (USA) 77:4030-4034 (1980); EP 52,322; EP 36,676; EP 88,046; EP 143,949; EP 142,641; Japanese Pat. Appl. 83-118008; U.S. Pat. Nos. 4,485,045 and 4,544,545; and EP 102,324. Ordinarily, the liposomes are of the small (about 200-800 Angstroms) unilamellar type in which the lipid content is greater than about 30 mol. percent cholesterol, the selected proportion being adjusted for the optimal Therapeutic.

In yet an additional embodiment, the Therapeutics of the invention are delivered by way of a pump (see Langer, supra; Sefton, CRC Crit. Ref. Biomed. Eng. 14:201 (1987); Buchwald et al., Surgery 88:507 (1980); Saudek et al., N. Engl. J. Med. 321:574 (1989)).

Other controlled release systems are discussed in the review by Langer (Science 249:1527-1533 (1990)).

For parenteral administration, in one embodiment, the Therapeutic is formulated generally by mixing it at the desired degree of purity, in a unit dosage injectable form (solution, suspension, or emulsion), with a pharmaceutically acceptable carrier, i.e., one that is non-toxic to recipients at the dosages and concentrations employed and is compatible with other ingredients of the formulation. For example, the formulation preferably does not include oxidizing agents and other compounds that are known to be deleterious to the Therapeutic.

Generally, the formulations are prepared by contacting the Therapeutic uniformly and intimately with liquid carriers or finely divided solid carriers or both. Then, if necessary, the product is shaped into the desired formulation. Preferably the carrier is a parenteral carrier, more preferably a solution that is isotonic with the blood of the recipient. Examples of such carrier vehicles include water, saline, Ringer's solution, and dextrose solution. Non-aqueous vehicles such as fixed oils and ethyl oleate are also useful herein, as well as liposomes.

The carrier suitably contains minor amounts of additives such as substances that enhance isotonicity and chemical stability. Such materials are non-toxic to recipients at the dosages and concentrations employed, and include buffers such as phosphate, citrate, succinate, acetic acid, and other organic acids or their salts; antioxidants such as ascorbic acid; low molecular weight (less than about ten residues) polypeptides, e.g., polyarginine or tripeptides; proteins, such as serum albumin, gelatin, or immunoglobulins; hydrophilic polymers such as polyvinylpyrrolidone; amino acids, such as glycine, glutamic acid, aspartic acid, or arginine; monosaccharides, disaccharides, and other carbohydrates including cellulose or its derivatives, glucose, manose, or dextrins; chelating agents such as EDTA; sugar alcohols such as mannitol or sorbitol; counterions such as sodium; and/or nonionic surfactants such as polysorbates, poloxamers, or PEG.

The Therapeutic is typically formulated in such vehicles at a concentration of about 0.1 mg/ml to 100 mg/ml, preferably 1-10 mg/ml, at a pH of about 3 to 8. It will be understood that the use of certain of the foregoing excipients, carriers, or stabilizers will result in the formation of polypeptide salts.

Any pharmaceutical used for therapeutic administration can be sterile. Sterility is readily accomplished by filtration through sterile filtration membranes (e.g., 0.2 micron membranes). Therapeutics generally are placed into a container having a sterile access port, for example, an intravenous solution bag or vial having a stopper pierceable by a hypodermic injection needle.

Therapeutics ordinarily will be stored in unit or multi-dose containers, for example, sealed ampoules or vials, as an aqueous solution or as a lyophilized formulation for reconstitution. As an example of a lyophilized formulation, 10-ml vials are filled with 5 ml of sterile-filtered 1% (w/v) aqueous Therapeutic solution, and the resulting mixture is lyophilized. The infusion solution is prepared by reconstituting the lyophilized Therapeutic using bacteriostatic Water-for-Injection.

The invention also provides a pharmaceutical pack or kit comprising one or more containers filled with one or more of the ingredients of the Therapeutics of the invention. Associated with such container(s) can be a notice in the form prescribed by a governmental agency regulating the manufacture, use or sale of pharmaceuticals or biological products, which notice reflects approval by the agency of manufacture, use or sale for human administration. In addition, the Therapeutics may be employed in conjunction with other therapeutic compounds.

The Therapeutics of the invention may be administered alone or in combination with adjuvants. Adjuvants that may be administered with the Therapeutics of the invention include, but are not limited to, alum, alum plus deoxycholate (ImmunoAg), MTP-PE (Biocine Corp.), QS21 (GENENTECH™, Inc.), BCG (e.g., THERACYS®), MPL and nonviable prepartions of Corynebacterium parvum. In a specific embodiment, Therapeutics of the invention are administered in combination with alum. In another specific embodiment, Therapeutics of the invention are administered in combination with QS-21. Further adjuvants that may be administered with the Therapeutics of the invention include, but are not limited to, Monophosphoryl lipid immunomodulator, AdjuVax 100a, QS-21, QS-18, CRL1005, Aluminum salts, MF-59, and Virosomal adjuvant technology. Vaccines that may be administered with the Therapeutics of the invention include, but are not limited to, vaccines directed toward protection against MMR (measles, mumps, rubella), polio, varicella, tetanus/diptheria, hepatitis A, hepatitis B, haemophilus influenzae B, whooping cough, pneumonia, influenza, Lyme's Disease, rotavirus, cholera, yellow fever, Japanese encephalitis, poliomyelitis, rabies, typhoid fever, and pertussis. Combinations may be administered either concomitantly, e.g., as an admixture, separately but simultaneously or concurrently; or sequentially. This includes presentations in which the combined agents are administered together as a therapeutic mixture, and also procedures in which the combined agents are administered separately but simultaneously, e.g., as through separate intravenous lines into the same individual. Administration “in combination” further includes the separate administration of one of the compounds or agents given first, followed by the second.

The Therapeutics of the invention may be administered alone or in combination with other therapeutic agents. Therapeutic agents that may be administered in combination with the Therapeutics of the invention, include but not limited to, chemotherapeutic agents, antibiotics, steroidal and non-steroidal anti-inflammatories, conventional immunotherapeutic agents, and/or therapeutic treatments described below. Combinations may be administered either concomitantly, e.g., as an admixture, separately but simultaneously or concurrently; or sequentially. This includes presentations in which the combined agents are administered together as a therapeutic mixture, and also procedures in which the combined agents are administered separately but simultaneously, e.g., as through separate intravenous lines into the same individual. Administration “in combination” further includes the separate administration of one of the compounds or agents given first, followed by the second.

In one embodiment, the Therapeutics of the invention are administered in combination with an anticoagulant. Anticoagulants that may be administered with the compositions of the invention include, but are not limited to, heparin, low molecular weight heparin, warfarin sodium (e.g., COUMADIN®), dicumarol, 4-hydroxycoumarin, anisindione (e.g., MIRADON™), acenocoumarol (e.g., nicoumalone, SINTHROME™), indan-1,3-dione, phenprocoumon (e.g., MARCUMAR™), ethyl biscoumacetate (e.g., TROMEXAN™), and aspirin. In a specific embodiment, compositions of the invention are administered in combination with heparin and/or warfarin. In another specific embodiment, compositions of the invention are administered in combination with warfarin. In another specific embodiment, compositions of the invention are administered in combination with warfarin and aspirin. In another specific embodiment, compositions of the invention are administered in combination with heparin. In another specific embodiment, compositions of the invention are administered in combination with heparin and aspirin.

In another embodiment, the Therapeutics of the invention are administered in combination with thrombolytic drugs. Thrombolytic drugs that may be administered with the compositions of the invention include, but are not limited to, plasminogen, lys-plasminogen, alpha2-antiplasmin, streptokinae (e.g., KABIKINASE™), antiresplace (e.g., EMINASE™), tissue plasminogen activator (t-PA, altevase, ACTIVASE™), urokinase (e.g., ABBOKINASE™), sauruplase, (Prourokinase, single chain urokinase), and aminocaproic acid (e.g., AMICAR™). In a specific embodiment, compositions of the invention are administered in combination with tissue plasminogen activator and aspirin.

In another embodiment, the Therapeutics of the invention are administered in combination with antiplatelet drugs. Antiplatelet drugs that may be administered with the compositions of the invention include, but are not limited to, aspirin, dipyridamole (e.g., PERSANTINE™), and ticlopidine (e.g., TICLID™).

In specific embodiments, the use of anti-coagulants, thrombolytic and/or antiplatelet drugs in combination with Therapeutics of the invention is contemplated for the detection, prevention, diagnosis, prognostication, treatment, and/or amelioration of thrombosis, arterial thrombosis, venous thrombosis, thromboembolism, pulmonary embolism, atherosclerosis, myocardial infarction, transient ischemic at ack, unstable angina. In specific embodiments, the use of anticoagulants, thrombolytic drugs and/or antiplatelet drugs in combination with Therapeutics of the invention is contemplated for the prevention of occulsion of saphenous grafts, for reducing the risk of periprocedural thrombosis as might accompany angioplasty procedures, for reducing the risk of stroke in patients with atrial fibrillation including nonrheumatic atrial fibrillation, for reducing the risk of embolism associated with mechanical heart valves and or mitral valves disease. Other uses for the therapeutics of the invention, alone or in combination with antiplatelet, anticoagulant, and/or thrombolytic drugs, include, but are not limited to, the prevention of occlusions in extracorporeal devices (e.g., intravascular canulas, vascular access shunts in hemodialysis patients, hemodialysis machines, and cardiopulmonary bypass machines).

In certain embodiments, Therapeutics of the invention are administered in combination with antiretroviral agents, nucleoside/nucleotide reverse transcriptase inhibitors (NRTIs), non-nucleoside reverse transcriptase inhibitors (NNRTIs), and/or protease inhibitors (PIs). NRTIs that may be administered in combination with the Therapeutics of the invention, include, but are not limited to, RETROVIR™ (zidovudine/AZT), VIDEX™ (didanosine/ddI), HIVID™ (zalcitabine/ddC), ZERIT™ (stavudine/d4T), EPIVIR™ (lamivudine/3TC), and COMBIVIR™ (zidovudine/lamivudine). NNRTIs that may be administered in combination with the Therapeutics of the invention, include, but are not limited to, VIRAMUNE™ (nevirapine), RESCRIPTOR™ (delavirdine), and SUSTIVA™ (efavirenz). Protease inhibitors that may be administered in combination with the Therapeutics of the invention, include, but are not limited to, CRIXIVAN™ (indinavir), NORVIR™ (ritonavir), INVIRASE™ (saquinavir), and VIRACEPT™ (nelfinavir). In a specific embodiment, antiretroviral agents, nucleoside reverse transcriptase inhibitors, non-nucleoside reverse transcriptase inhibitors, and/or protease inhibitors may be used in any combination with Therapeutics of the invention to treat AIDS and/or to prevent or treat HIV infection.

Additional NRTIs include LODENOSINE™ (F-ddA; an acid-stable adenosine NRTI; Triangle/ABBOTT™; COVIRACIL™ (emtricitabine/FTC; structurally related to lamivudine (3TC) but with 3- to 10-fold greater activity in vitro; Triangle/ABBOTT™); dOTC (BCH-10652, also structurally related to lamivudine but retains activity against a substantial proportion of lamivudine-resistant isolates; Biochem Pharma); Adefovir (refused approval for anti-HIV therapy by FDA; Gilead Sciences); PREVEON® (Adefovir Dipivoxil, the active prodrug of adefovir; its active form is PMEA-pp); TENOFOVIR™ (bis-POC PMPA, a PMPA prodrug; Gilead); DAPD/DXG (active metabolite of DAPD; Triangle/ABBOTT™); D-D4FC (related to 3TC, with activity against AZT/3TC-resistant virus); GW420867X (Glaxo Wellcome); ZIAGEN™ (abacavir/159U89; Glaxo Wellcome Inc.); CS-87 (3′azido-2′,3′-dideoxyuridine; WO 99/66936); and S-acyl-2-thioethyl (SATE)-bearing prodrug forms of β-L-FD4C and β-L-FddC (WO 98/17281).

Additional NNRTIs include COACTINON™ (Emivirine/MKC-442, potent NNRTI of the HEPT class; Triangle/ABBOTT™); CAPRAVIRINE™ (AG-1549/S-1153, a next generation NNRTI with activity against viruses containing the K103N mutation; AGOURON™); PNU-142721 (has 20- to 50-fold greater activity than its predecessor delavirdine and is active against K103N mutants; PHARMACIA™ & Upjohn); DPC-961 and DPC-963 (second-generation derivatives of efavirenz, designed to be active against viruses with the K103N mutation; DUPONT™); GW-420867X (has 25-fold greater activity than HBY097 and is active against K103N mutants; Glaxo Wellcome); CALANOLIDE A (naturally occurring agent from the latex tree; active against viruses containing either or both the Y181C and K103N mutations); and Propolis (WO 99/49830).

Additional protease inhibitors include LOPINAVIR™ (ABT378/r; ABBOTT™ Laboratories); BMS-232632 (an azapeptide; BRISTOL-MYERS SQUIBB™); TIPRANAVIR™ (PNU-140690, a non-peptic dihydropyrone; PHARMACIA™ & Upjohn); PD-178390 (a nonpeptidic dihydropyrone; Parke-Davis); BMS 232632 (an azapeptide; BRISTOL-MYERS SQUIBB™); L-756,423 (an indinavir analog; MERCK™); DMP-450 (a cyclic urea compound; Avid & DUPONT™); AG-1776 (a peptidomimetic with in vitro activity against protease inhibitor-resistant viruses; AGOURON™); VX-175/GW-433908 (phosphate prodrug of amprenavir; Vertex & Glaxo Welcome); CGP61755 (Ciba); and AGENERASE™ (amprenavir; Glaxo Wellcome Inc.).

Additional antiretroviral agents include fusion inhibitors/gp41 binders. Fusion inhibitors/gp41 binders include T-20 (a peptide from residues 643-678 of the HIV gp41 transmembrane protein ectodomain which binds to gp41 in its resting state and prevents transformation to the fusogenic state; Trimeris) and T-1249 (a second-generation fusion inhibitor; Trimeris).

Additional antiretroviral agents include fusion inhibitors/chemokine receptor antagonists. Fusion inhibitors/chemokine receptor antagonists include CXCR4 antagonists such as AMD 3100 (a bicyclam), SDF-1 and its analogs, and ALX40-4C (a cationic peptide), T22 (an 18 amino acid peptide; Trimeris) and the T22 analogs T134 and T140; CCR5 antagonists such as RANTES (9-68), AOP-RANTES, NNY-RANTES, and TAK-779; and CCR5/CXCR4 antagonists such as NSC 651016 (a distamycin analog). Also included are CCR2B, CCR3, and CCR6 antagonists. Chemokine receptor agonists such as RANTES, SDF-1, MIP-1α, MIP-1β, etc., may also inhibit fusion.

Additional antiretroviral agents include integrase inhibitors. Integrase inhibitors include dicaffeoylquinic (DFQA) acids; L-chicoric acid (a dicaffeoyltartaric (DCTA) acid); quinalizarin (QLC) and related anthraquinones; ZINTEVIR™ (AR 177, an oligonucleotide that probably acts at cell surface rather than being a true integrase inhibitor; Arondex); and naphthols such as those disclosed in WO 98/50347.

Additional antiretroviral agents include hydroxyurea-like compounds such as BCX-34 (a purine nucleoside phosphorylase inhibitor; Biocryst); ribonucleotide reductase inhibitors such as DIDOX™ (Molecules for Health); inosine monophosphate dehydrogenase (IMPDH) inhibitors such a as VX-497 (Vertex); and mycopholic acids such as CellCept (mycophenolate mofetil; ROCHE™).

Additional antiretroviral agents include inhibitors of viral integrase, inhibitors of viral genome nuclear translocation such as arylene bis(methylketone) compounds; inhibitors of HIV entry such as AOP-RANTES, NNY-RANTES, RANTES-IgG fusion protein, soluble complexes of RANTES and glycosaminoglycans (GAG), and AMD-3100; nucleocapsid zinc finger inhibitors such as dithiane compounds; targets of HIV Tat and Rev; and pharmacoenhancers such as ABT-378.

Other antiretroviral therapies and adjunct therapies include cytokines and lymphokines such as MIP-1α, MIP-1β, SDF-1α, IL-2, PROLEUKIN™ (aldesleukin/L2-7001; CHIRON™), IL-4, IL-10, IL-12, and IL-13; interferons such as IFN-α2a; antagonists of TNFs, NFκB, GM-CSF, M-CSF, and IL-10; agents that modulate immune activation such as cyclosporin and prednisone; vaccines such as Remune™ (HIV Immunogen), APL 400-003 (Apollon), recombinant gp120 and fragments, bivalent (B/E) recombinant envelope glycoprotein, rgp120CM235, MN rgp120, SF-2 rgp120, gp120/soluble CD4 complex, Delta JR-FL protein, branched synthetic peptide derived from discontinuous gp120 C3/C4 domain, fusion-competent immunogens, and Gag, Pol, Nef, and Tat vaccines; gene-based therapies such as genetic suppressor elements (GSEs; WO 98/54366), and intrakines (genetically modified CC chemokines targetted to the ER to block surface expression of newly synthesized CCR5 (Yang et al., PNAS 94:11567-72 (1997); Chen et al., Nat. Med. 3:1110-16 (1997)); antibodies such as the anti-CXCR4 antibody 12G5, the anti-CCR5 antibodies 2D7, 5C7, PA8, PA9, PA10, PA11, PA12, and PA14, the anti-CD4 antibodies Q4120 and RPA-T4, the anti-CCR3 antibody 7B11, the anti-gp120 antibodies 17b, 48d, 447-52D, 257-D, 268-D and 50.1, anti-Tat antibodies, anti-TNF-α antibodies, and monoclonal antibody 33A; aryl hydrocarbon (AH) receptor agonists and antagonists such as TCDD, 3,3′,4,4′,5-pentachlorobiphenyl, 3,3′,4,4′-tetrachlorobiphenyl, and α-naphthoflavone (WO 98/30213); and antioxidants such as γ-L-glutamyl-L-cysteine ethyl ester (γ-GCE; WO 99/56764).

In a further embodiment, the Therapeutics of the invention are administered in combination with an antiviral agent. Antiviral agents that may be administered with the Therapeutics of the invention include, but are not limited to, acyclovir, ribavirin, amantadine, and remantidine.

In other embodiments, Therapeutics of the invention may be administered in combination with anti-opportunistic infection agents. Anti-opportunistic agents that may be administered in combination with the Therapeutics of the invention, include, but are not limited to, TRIMETHOPRIM-SULFAMETHOXAZOLE™, DAPSONE™, PENTAMIDINE™, ATOVAQUONE™, ISONIAZID™, RIFAMPIN™, PYRAZINAMIDE™, ETHAMBUTOL™, RIFABUTIN™, CLARITHROMYCIN™, AZITHROMYCIN™, GANCICLOVIR™, FOSCARNET™, CIDOFOVIR™, FLUCONAZOLE™, ITRACONAZOLE™, KETOCONAZOLE™, ACYCLOVIR™, FAMCICOLVIR™, PYRIMETHAMINE™, LEUCOVORIN™, NEUPOGEN™ (filgrastim/G-CSF), and LEUKINE™ (sargramostim/GM-CSF). In a specific embodiment, Therapeutics of the invention are used in any combination with TRIMETHOPRIM-SULFAMETHOXAZOLE™, DAPSONE™, PENTAMIDINE™, and/or ATOVAQUONE™ to prophylactically treat or prevent an opportunistic Pneumocystis carinii pneumonia infection. In another specific embodiment, Therapeutics of the invention are used in any combination with ISONIAZID™, RIFAMPIN™, PYRAZINAMIDE™, and/or ETHAMBUTOL™ to prophylactically treat or prevent an opportunistic Mycobacterium avium complex infection. In another specific embodiment, Therapeutics of the invention are used in any combination with RIFABUTIN™, CLARITHROMYCIN™, and/or AZITHROMYCIN™ to prophylactically treat or prevent an opportunistic Mycobacterium tuberculosis infection. In another specific embodiment, Therapeutics of the invention are used in any combination with GANCICLOVIR™, FOSCARNET™, and/or CIDOFOVIR™ to prophylactically treat or prevent an opportunistic cytomegalovirus infection. In another specific embodiment, Therapeutics of the invention are used in any combination with FLUCONAZOLE™, ITRACONAZOLE™, and/or KETOCONAZOLE™ to prophylactically treat or prevent an opportunistic fungal infection. In another specific embodiment, Therapeutics of the invention are used in any combination with ACYCLOVIR™ and/or FAMCICOLVIR™ to prophylactically treat or prevent an opportunistic herpes simplex virus type I and/or type II infection. In another specific embodiment, Therapeutics of the invention are used in any combination with PYRIMETHAMINE™ and/or LEUCOVORIN™ to prophylactically treat or prevent an opportunistic Toxoplasma gondii infection. In another specific embodiment, Therapeutics of the invention are used in any combination with LEUCOVORIN™ and/or NEUPOGEN™ to prophylactically treat or prevent an opportunistic bacterial infection.

In a further embodiment, the Therapeutics of the invention are administered in combination with an antibiotic agent. Antibiotic agents that may be administered with the Therapeutics of the invention include, but are not limited to, amoxicillin, beta-lactamases, aminoglycosides, beta-lactam (glycopeptide), beta-lactamases, Clindamycin, chloramphenicol, cephalosporins, ciprofloxacin, erythromycin, fluoroquinolones, macrolides, metronidazole, penicillins, quinolones, rapamycin, rifampin, streptomycin, sulfonamide, tetracyclines, trimethoprim, trimethoprim-sulfamethoxazole, and vancomycin.

In other embodiments, the Therapeutics of the invention are administered in combination with immunestimulants. Immunostimulants that may be administered in combination with the Therapeutics of the invention include, but are not limited to, levamisole (e.g., ERGAMISOL™), isoprinosine (e.g. INOSIPLEX™), interferons (e.g. interferon alpha), and interleukins (e.g., IL-2).

In other embodiments, Therapeutics of the invention are administered in combination with immunosuppressive agents. Immunosuppressive agents that may be administered in combination with the Therapeutics of the invention include, but are not limited to, steroids, cyclosporine, cyclosporine analogs, cyclophosphamide methylprednisone, prednisone, azathioprine, FK-506, 15-deoxyspergualin, and other immunosuppressive agents that act by suppressing the function of responding T cells. Other immunosuppressive agents that may be administered in combination with the Therapeutics of the invention include, but are not limited to, prednisolone, methotrexate, thalidomide, methoxsalen, rapamycin, leflunomide, mizoribine (BREDININ™), brequinar, deoxyspergualin, and azaspirane (SKF 105685), ORTHOCLONE OKT® 3 (muromonab-CD3), SANDIMMUNE™, NEORAL™, SANGDYA™ (cyclosporine), PROGRAF® (FK506, tacrolimus), CELLCEPT® (mycophenolate motefil, of which the active metabolite is mycophenolic acid), IMURAN™ (azathioprine), glucocorticosteroids, adrenocortical steroids such as DELTASONE™ (prednisone) and HYDELTRASOL™ (prednisolone), FOLEX™ and MEXATE™ (methotrxate), OXSORALEN-ULTRA™ (methoxsalen) and RAPAMUNE™ (sirolimus). In a specific embodiment, immunosuppressants may be used to prevent rejection of organ or bone marrow transplantation.

In an additional embodiment, Therapeutics of the invention are administered alone or in combination with one or more intravenous immune globulin preparations. Intravenous immune globulin preparations that may be administered with the Therapeutics of the invention include, but not limited to, GAMMAR™, IVEEGAM™, SANDOGLOBULIN™, GAMMAGARD S/D™, ATGAM™ (antithymocyte glubulin), and GAMIMUNE™. In a specific embodiment, Therapeutics of the invention are administered in combination with intravenous immune globulin preparations in transplantation therapy (e.g., bone marrow transplant).

In certain embodiments, the Therapeutics of the invention are administered alone or in combination with an anti-inflammatory agent. Anti-inflammatory agents that may be administered with the Therapeutics of the invention include, but are not limited to, corticosteroids (e.g. betamethasone, budesonide, cortisone, dexamethasone, hydrocortisone, methylprednisolone, prednisolone, prednisone, and triamcinolone), nonsteroidal anti-inflammatory drugs (e.g., diclofenac, diflunisal, etodolac, fenoprofen, floctafenine, flurbiprofen, ibuprofen, indomethacin, ketoprofen, meclofenamate, mefenamic acid, meloxicam, nabumetone, naproxen, oxaprozin, phenylbutazone, piroxicam, sulindac, tenoxicam, tiaprofenic acid, and tolmetin.), as well as antihistamines, aminoarylcarboxylic acid derivatives, arylacetic acid derivatives, arylbutyric acid derivatives, arylcarboxylic acids, arylpropionic acid derivatives, pyrazoles, pyrazolones, salicylic acid derivatives, thiazinecarboxamides, e-acetamidocaproic acid, S-adenosylmethionine, 3-amino-4-hydroxybutyric acid, amixetrine, bendazac, benzydamine, bucolome, difenpiramide, ditazol, emorfazone, guaiazulene, nabumetone, nimesulide, orgotein, oxaceprol, paranyline, perisoxal, pifoxime, proquazone, proxazole, and tenidap.

In an additional embodiment, the compositions of the invention are administered alone or in combination with an anti-angiogenic agent. Anti-angiogenic agents that may be administered with the compositions of the invention include, but are not limited to, Angiostatin (ENTREMED™, Rockville, Md.), Troponin-1 (Boston Life Sciences, Boston, Mass.), anti-Invasive Factor, retinoic acid and derivatives thereof, paclitaxel (TAXOL™), Suramin, Tissue Inhibitor of Metalloproteinase-1, Tissue Inhibitor of Metalloproteinase-2, VEGI, Plasminogen Activator Inhibitor-1, Plasminogen Activator Inhibitor-2, and various forms of the lighter “d group” transition metals.

Lighter “d group” transition metals include, for example, vanadium, molybdenum, tungsten, titanium, niobium, and tantalum species. Such transition metal species may form transition metal complexes. Suitable complexes of the above-mentioned transition metal species include oxo transition metal complexes.

Representative examples of vanadium complexes include oxo vanadium complexes such as vanadate and vanadyl complexes. Suitable vanadate complexes include metavanadate and orthovanadate complexes such as, for example, ammonium metavanadate, sodium metavanadate, and sodium orthovanadate. Suitable vanadyl complexes include, for example, vanadyl acetylacetonate and vanadyl sulfate including vanadyl sulfate hydrates such as vanadyl sulfate mono- and trihydrates.

Representative examples of tungsten and molybdenum complexes also include oxo complexes. Suitable oxo tungsten complexes include tungstate and tungsten oxide complexes. Suitable tungstate complexes include ammonium tungstate, calcium tungstate, sodium tungstate dihydrate, and tungstic acid. Suitable tungsten oxides include tungsten (IV) oxide and tungsten (VI) oxide. Suitable oxo molybdenum complexes include molybdate, molybdenum oxide, and molybdenyl complexes. Suitable molybdate complexes include ammonium molybdate and its hydrates, sodium molybdate and its hydrates, and potassium molybdate and its hydrates. Suitable molybdenum oxides include molybdenum (VI) oxide, molybdenum (VI) oxide, and molybdic acid. Suitable molybdenyl complexes include, for example, molybdenyl acetylacetonate. Other suitable tungsten and molybdenum complexes include hydroxo derivatives derived from, for example, glycerol, tartaric acid, and sugars.

A wide variety of other anti-angiogenic factors may also be utilized within the context of the present invention. Representative examples include, but are not limited to, platelet factor 4; protamine sulphate; sulphated chitin derivatives (prepared from queen crab shells), (Murata et al., Cancer Res. 51:22-26, (1991)); Sulphated Polysaccharide Peptidoglycan Complex (SP-PG) (the function of this compound may be enhanced by the presence of steroids such as estrogen, and tamoxifen citrate); Staurosporine; modulators of matrix metabolism, including for example, proline analogs, cishydroxyproline, d,L-3,4-dehydroproline, Thiaproline, alpha,alpha-dipyridyl, aminopropionitrile fumarate; 4-propyl-5-(4-pyridinyl)-2(3H)-oxazolone; Methotrexate; Mitoxantrone; Heparin; Interferons; 2 Macroglobulin-serum; ChIMP-3 (Pavloff et al., J. Bio. Chem. 267:17321-17326, (1992)); Chymostatin (Tomkinson et al., Biochem J. 286:475-480, (1992)); Cyclodextrin Tetradecasulfate; Eponemycin; Camptothecin; Fumagillin (Ingber et al., Nature 348:555-557, (1990)); Gold Sodium Thiomalate (“GST”; Matsubara and Ziff, J. Clin. Invest. 79:1440-1446, (1987)); anticollagenase-serum; alpha2-antiplasmin (Holmes et al., J. Biol. Chem. 262(4):1659-1664, (1987)); Bisantrene (National Cancer Institute); Lobenzarit disodium (N-(2)-carboxyphenyl-4-chloroanthronilic acid disodium or “CCA”; (Takeuchi et al., Agents Actions 36:312-316, (1992)); and metalloproteinase inhibitors such as BB94.

Additional anti-angiogenic factors that may also be utilized within the context of the present invention include Thalidomide, (CELGENE™, Warren, N.J.); Angiostatic steroid; AGM-1470 (H. Brem and J. Folkman J Pediatr. Surg. 28:445-51 (1993)); an integrin alpha v beta 3 antagonist (C. Storgard et al., J. Clin. Invest. 103:47-54 (1999)); carboxynaminolmidazole; Carboxyamidotriazole (CAI) (National Cancer Institute, Bethesda, Md.); Conbretastatin A-4 (CA4P) (OXIGENE™, Boston, Mass.); Squalamine (Magainin Pharmaceuticals, Plymouth Meeting, Pa.); TNP-470, (TAP PHARMACEUTICALS™, Deerfield, Ill.); ZD-0101 ASTRAZENECA™ (London, UK); APRA (CT2584); Benefin, Byrostatin-1 (SC339555); CGP-41251 (PKC 412); CM101; Dexrazoxane (ICRF187); DMXAA; Endostatin; Flavopridiol; Genestein; GTE; ImmTher; Iressa (ZD1839); Octreotide (Somatostatin); Panretin; Penacillamine; Photopoint; PI-88; Prinomastat (AG-3340) Purlytin; Suradista (FCE26644); Tamoxifen (OLVADEX™); Tazarotene; Tetrathiomolybdate; XELODA™ (Capecitabine); and 5-Fluorouracil.

Anti-angiogenic agents that may be administered in combination with the compounds of the invention may work through a variety of mechanisms including, but not limited to, inhibiting proteolysis of the extracellular matrix, blocking the function of endothelial cell-extracellular matrix adhesion molecules, by antagonizing the function of angiogenesis inducers such as growth factors, and inhibiting integrin receptors expressed on proliferating endothelial cells. Examples of anti-angiogenic inhibitors that interfere with extracellular matrix proteolysis and which may be administered in combination with the compositions of the invention include, but are not limited to, AG-3340 (AGOURON™, La Jolla, Calif.), BAY-12-9566 (BAYER™, West Haven, Conn.), BMS-275291 (BRISTOL-MYERS SQUIBB™, Princeton, N.J.), CGS-27032A (OVARTIS™, East Hanover, N.J.), Marimastat (British Biotech, Oxford, UK), and METASTAT™ (AETERNA™, St-Foy, Quebec). Examples of anti-angiogenic inhibitors that act by blocking the function of endothelial cell-extracellular matrix adhesion molecules and which may be administered in combination with the compositons of the invention include, but are not lmited to, EMD-121974 (MERCK™ KcgaA Darmstadt, Germany) and VITAXIN™ (IXSYS™, La Jolla, Calif./MEDIMMUNE™, Gaithersburg, Md.). Examples of anti-angiogenic agents that act by directly antagonizing or inhibiting angiogenesis inducers and which may be administered in combination with the compositons of the invention include, but are not lmited to, Angiozyme (Ribozyme, Boulder, Colo.), Anti-VEGF antibody (GENENTECH™, S. San Francisco, Calif.), PTK-787/ZK-225846 (OVARTIS™, Base1, Switzerland), SU-101 (SUGEN™, S. San Francisco, Calif.), SU-5416 (SUGEN™/PHARMACIA™

Upjohn, Bridgewater, N.J.), and SU-6668 (SUGEN™). Other anti-angiogenic agents act to indirectly inhibit angiogenesis. Examples of indirect inhibitors of angiogenesis which may be administered in combination with the compositions of the invention include, but are not limited to, IM-862 (CYTRAN™, Kirkland, Wash.), Interferon-alpha, IL-12 (ROCHE™, Nutley, N.J.), and Pentosan polysulfate (Georgetown University, Washington, D.C.).

In particular embodiments, the use of compositions of the invention in combination with anti-angiogenic agents is contemplated for the treatment, prevention, and/or amelioration of an autoimmune disease, such as for example, an autoimmune disease described herein.

In a particular embodiment, the use of compositions of the invention in combination with anti-angiogenic agents is contemplated for the treatment, prevention, and/or amelioration of arthritis. In a more particular embodiment, the use of compositions of the invention in combination with anti-angiogenic agents is contemplated for the treatment, prevention, and/or amelioration of rheumatoid arthritis.

In another embodiment, the polynucleotides encoding a polypeptide of the present invention are administered in combination with an angiogenic protein, or polynucleotides encoding an angiogenic protein. Examples of angiogenic proteins that may be administered with the compositions of the invention include, but are not limited to, acidic and basic fibroblast growth factors, VEGF-1, VEGF-2, VEGF-3, epidermal growth factor alpha and beta, platelet-derived endothelial cell growth factor, platelet-derived growth factor, tumor necrosis factor alpha, hepatocyte growth factor, insulin-like growth factor, colony stimulating factor, macrophage colony stimulating factor, granulocyte/macrophage colony stimulating factor, and nitric oxide synthase.

In additional embodiments, compositions of the invention are administered in combination with a chemotherapeutic agent. Chemotherapeutic agents that may be administered with the Therapeutics of the invention include, but are not limited to alkylating agents such as nitrogen mustards (for example, Mechlorethamine, cyclophosphamide, Cyclophosphamide Ifosfamide, Melphalan (L-sarcolysin), and Chlorambucil), ethylenimines and methylmelamines (for example, Hexamethylmelamine and Thiotepa), alkyl sulfonates (for example, Busulfan), nitrosoureas (for example, Carmustine (BCNU), Lomustine (CCNU), Semustine (methyl-CCNU), and Streptozocin (streptozotocin)), triazenes (for example, Dacarbazine (DTIC; dimethyltriazenoimidazolecarboxamide)), folic acid analogs (for example, Methotrexate (amethopterin)), pyrimidine analogs (for example, Fluorouacil (5-fluorouracil; 5-FU), Floxuridine (fluorodeoxyuridine; FudR), and Cytarabine (cytosine arabinoside)), purine analogs and related inhibitors (for example, Mercaptopurine (6-mercaptopurine; 6-MP), Thioguanine (6-thioguanine; TG), and Pentostatin (2′-deoxycoformycin)), vinca alkaloids (for example, Vinblastine (VLB, vinblastine sulfate)) and Vincristine (vincristine sulfate)), epipodophyllotoxins (for example, Etoposide and Teniposide), antibiotics (for example, Dactinomycin (actinomycin D), Daunorubicin (daunomycin; rubidomycin), Doxorubicin, Bleomycin, Plicamycin (mithramycin), and Mitomycin (mitomycin C), enzymes (for example, L-Asparaginase), biological response modifiers (for example, Interferon-alpha and interferon-alpha-2b), platinum coordination compounds (for example, Cisplatin (cis-DDP) and Carboplatin), anthracenedione (Mitoxantrone), substituted ureas (for example, Hydroxyurea), methylhydrazine derivatives (for example, Procarbazine (N-methylhydrazine; MIH), adrenocorticosteroids (for example, Prednisone), progestins (for example, Hydroxyprogesterone caproate, Medroxyprogesterone, Medroxyprogesterone acetate, and Megestrol acetate), estrogens (for example, Diethylstilbestrol (DES), Diethylstilbestrol diphosphate, Estradiol, and Ethinyl estradiol), antiestrogens (for example, Tamoxifen), androgens (Testosterone proprionate, and Fluoxymesterone), antiandrogens (for example, Flutamide), gonadotropin-releasing hormone analogs (for example, Leuprolide), other hormones and hormone analogs (for example, methyltestosterone, estramustine, estramustine phosphate sodium, chlorotrianisene, and testolactone), and others (for example, dicarbazine, glutamic acid, and mitotane).

In one embodiment, the compositions of the invention are administered in combination with one or more of the following drugs: infliximab (also known as Remicade™ Centocor, Inc.), Trocade (ROCHE™, RO-32-3555), Leflunomide (also known as Arava™ from HOECHST MARION ROUSSEL™), Kineret™ (an IL-1 Receptor antagonist also known as Anakinra from AMGEN™, Inc.)

In a specific embodiment, compositions of the invention are administered in combination with CHOP (cyclophosphamide, doxorubicin, vincristine, and prednisone) or combination of one or more of the components of CHOP. In one embodiment, the compositions of the invention are administered in combination with anti-CD20 antibodies, human monoclonal anti-CD20 antibodies. In another embodiment, the compositions of the invention are administered in combination with anti-CD20 antibodies and CHOP, or anti-CD20 antibodies and any combination of one or more of the components of CHOP, particularly cyclophosphamide and/or prednisone. In a specific embodiment, compositions of the invention are administered in combination with Rituximab. In a further embodiment, compositions of the invention are administered with Rituximab and CHOP, or Rituximab and any combination of one or more of the components of CHOP, particularly cyclophosphamide and/or prednisone. In a specific embodiment, compositions of the invention are administered in combination with tositumomab. In a further embodiment, compositions of the invention are administered with tositumomab and CHOP, or tositumomab and any combination of one or more of the components of CHOP, particularly cyclophosphamide and/or prednisone. The anti-CD20 antibodies may optionally be associated with radioisotopes, toxins or cytotoxic prodrugs.

In another specific embodiment, the compositions of the invention are administered in combination Zevalin™. In a further embodiment, compositions of the invention are administered with Zevalin™ and CHOP, or Zevalin™ and any combination of one or more of the components of CHOP, particularly cyclophosphamide and/or prednisone. Zevalin™ may be associated with one or more radioisotopes. Particularly preferred isotopes are ⁹⁰Y and ¹¹¹In.

In an additional embodiment, the Therapeutics of the invention are administered in combination with cytokines. Cytokines that may be administered with the Therapeutics of the invention include, but are not limited to, IL2, IL3, IL4, IL5, IL6, IL7, IL10, IL12, IL13, IL15, anti-CD40, CD40L, IFN-gamma and TNF-alpha. In another embodiment, Therapeutics of the invention may be administered with any interleukin, including, but not limited to, IL-1alpha, IL-1beta, IL-2, IL-3, IL-4, IL-5, IL-6, IL-7, IL-8, IL-9, IL-10, IL-11, IL-12, IL-13, IL-14, IL-15, IL-16, IL-17, IL-18, IL-19, IL-20, and IL-21.

In one embodiment, the Therapeutics of the invention are administered in combination with members of the TNF family. TNF, TNF-related or TNF-like molecules that may be administered with the Therapeutics of the invention include, but are not limited to, soluble forms of TNF-alpha, lymphotoxin-alpha (LT-alpha, also known as TNF-beta), LT-beta (found in complex heterotrimer LT-alpha2-beta), OPGL, FasL, CD27L, CD30L, CD40L, 4-IBBL, DcR3, OX40L, TNF-gamma (International Publication No. WO 96/14328), AIM-I (International Publication No. WO 97/33899), endokine-alpha (International Publication No. WO 98/07880), OPG, and neutrokine-alpha (International Publication No. WO 98/18921, OX40, and nerve growth factor (NGF), and soluble forms of Fas, CD30, CD27, CD40 and 4-IBB, TR2 (International Publication No. WO 96/34095), DR3 (International Publication No. WO 97/33904), DR4 (International Publication No. WO 98/32856), TR5 (International Publication No. WO 98/30693), TRANK, TR9 (International Publication No. WO 98/56892), TR10 (International Publication No. WO 98/54202), 312C2 (International Publication No. WO 98/06842), and TR12, and soluble forms CD154, CD70, and CD 153.

In an additional embodiment, the Therapeutics of the invention are administered in combination with angiogenic proteins. Angiogenic proteins that may be administered with the Therapeutics of the invention include, but are not limited to, Glioma Derived Growth Factor (GDGF), as disclosed in European Patent Number EP-399816; Platelet Derived Growth Factor-A (PDGF-A), as disclosed in European Patent Number EP-682110; Platelet Derived Growth Factor-B (PDGF-B), as disclosed in European Patent Number EP-282317; Placental Growth Factor (PlGF), as disclosed in International Publication Number WO 92/06194; Placental Growth Factor-2 (PlGF-2), as disclosed in Hauser et al., Growth Factors, 4:259-268 (1993); Vascular Endothelial Growth Factor (VEGF), as disclosed in International Publication Number WO 90/13649; Vascular Endothelial Growth Factor-A (VEGF-A), as disclosed in European Patent Number EP-506477; Vascular Endothelial Growth Factor-2 (VEGF-2), as disclosed in International Publication Number WO 96/39515; Vascular Endothelial Growth Factor B (VEGF-3); Vascular Endothelial Growth Factor B-186 (VEGF-B 186), as disclosed in International Publication Number WO 96/26736; Vascular Endothelial Growth Factor-D (VEGF-D), as disclosed in International Publication Number WO 98/02543; Vascular Endothelial Growth Factor-D (VEGF-D), as disclosed in International Publication Number WO 98/07832; and Vascular Endothelial Growth Factor-E (VEGF-E), as disclosed in German Patent Number DE19639601. The above mentioned references are herein incorporated by reference in their entireties.

In an additional embodiment, the Therapeutics of the invention are administered in combination with Fibroblast Growth Factors. Fibroblast Growth Factors that may be administered with the Therapeutics of the invention include, but are not limited to, FGF-1, FGF-2, FGF-3, FGF-4, FGF-5, FGF-6, FGF-7, FGF-8, FGF-9, FGF-10, FGF-11, FGF-12, FGF-13, FGF-14, and FGF-15.

In an additional embodiment, the Therapeutics of the invention are administered in combination with hematopoietic growth factors. Hematopoietic growth factors that may be administered with the Therapeutics of the invention include, but are not limited to, granulocyte macrophage colony stimulating factor (GM-CSF) (sargramostim, LEUKINE™, PROKINE™), granulocyte colony stimulating factor (G-CSF) (filgrastim, NEUPOGEN™), macrophage colony stimulating factor (M-CSF, CSF-1) erythropoietin (epoetin alfa, EPOGEN™, PROCRIT™), stem cell factor (SCF, c-kit ligand, steel factor), megakaryocyte colony stimulating factor, PIXY321 (a GMCSF/IL-3 fusion protein), interleukins, especially any one or more of IL-1 through IL-12, interferon-gamma, or thrombopoietin.

In certain embodiments, Therapeutics of the present invention are administered in combination with adrenergic blockers, such as, for example, acebutolol, atenolol, betaxolol, bisoprolol, carteolol, labetalol, metoprolol, nadolol, oxprenolol, penbutolol, pindolol, propranolol, sotalol, and timolol.

In another embodiment, the Therapeutics of the invention are administered in combination with an antiarrhythmic drug (e.g., adenosine, amidoarone, bretylium, digitalis, digoxin, digitoxin, diliazem, disopyramide, esmolol, flecamide, lidocaine, mexiletine, moricizine, phenyloin, procainamide, N-acetyl procainamide, propafenone, propranolol, quinidine, sotalol, tocamide, and verapamil).

In another embodiment, the Therapeutics of the invention are administered in combination with diuretic agents, such as carbonic anhydrase-inhibiting agents (e.g., acetazolamide, dichlorphenamide, and methazolamide), osmotic diuretics (e.g., glycerin, isosorbide, mannitol, and urea), diuretics that inhibit Na⁺—K⁺-2Cl⁻ symport (e.g., furosemide, bumetanide, azosemide, piretanide, tripamide, ethacrynic acid, muzolimine, and torsemide), thiazide and thiazide-like diuretics (e.g., bendroflumethiazide, benzthiazide, chlorothiazide, hydrochlorothiazide, hydroflumethiazide, methyclothiazide, polythiazide, trichormethiazide, chlorthalidone, indapamide, metolazone, and quinethazone), potassium sparing diuretics (e.g., amiloride and triamterene), and mineralcorticoid receptor antagonists (e.g., spironolactone, canrenone, and potassium canrenoate).

In one embodiment, the Therapeutics of the invention are administered in combination with treatments for endocrine and/or hormone imbalance disorders. Treatments for endocrine and/or hormone imbalance disorders include, but are not limited to, ¹²⁷I, radioactive isotopes of iodine such as ¹³¹I and ¹²³I; recombinant growth hormone, such as HUMATROPE™ (recombinant somatropin); growth hormone analogs such as PROTROPIN™ (somatrem); dopamine agonists such as PARLODEL™ (bromocriptine); somatostatin analogs such as SANDOSTATIN™ (octreotide); gonadotropin preparations such as PREGNYL™, A.P.L™ and PROFASI™ (chorionic gonadotropin (CG)), PERGONAL™ (menotropins), and METRODIN™ (urofollitropin (uFSH)); synthetic human gonadotropin releasing hormone preparations such as FACTREL™ and LUTREPULSE™ (gonadorelin hydrochloride); synthetic gonadotropin agonists such as LUPRON™ (leuprolide acetate), SUPPRELIN™ (histrelin acetate), SYNAREL™ (nafarelin acetate), and ZOLADEX™ (goserelin acetate); synthetic preparations of thyrotropin-releasing hormone such as RELEFACT TRH™ and THYPINONE™ (protirelin); recombinant human TSH such as THYROGEN™; synthetic preparations of the sodium salts of the natural isomers of thyroid hormones such as L-T₄™, SYNTHROID™ and LEVOTHROID™ (levothyroxine sodium), L-T₃™, CYTOMEL™ and TRIOSTAT™ (liothyroine sodium), and THYROLAR™ (liotrix); antithyroid compounds such as 6-n-propylthiouracil (propylthiouracil), 1-methyl-2-mercaptoimidazole and TAPAZOLE™ (methimazole), NEO-MERCAZOLE™ (carbimazole); beta-adrenergic receptor antagonists such as propranolol and esmolol; Ca²⁺ channel blockers; dexamethasone and iodinated radiological contrast agents such as TELEPAQUE™ (iopanoic acid) and ORAGRAFIN™ (sodium ipodate).

Additional treatments for endocrine and/or hormone imbalance disorders include, but are not limited to, estrogens or congugated estrogens such as ESTRACE™ (estradiol), ESTINYL™ (ethinyl estradiol), PREMARIN™, ESTRATAB™, ORTHO-EST™, OGEN™ and estropipate (estrone), ESTROVIS™ (quinestrol), ESTRADERM™ (estradiol), DELESTROGEN™ and VALERGEN™ (estradiol valerate), DEPO-ESTRADIOL CYPIONATE™ and ESTROJECT LA™ (estradiol cypionate); antiestrogens such as NOLVADEX™ (tamoxifen), SEROPHENE™ and CLOMID™ (clomiphene); progestins such as DURALUTIN™ (hydroxyprogesterone caproate), MPA™ and DEPO-PROVERA™ (medroxyprogesterone acetate), PROVERA™ and CYCRIN™ (MPA), MEGACE™ (megestrol acetate), NORLUTIN™ (norethindrone), and NORLUTATE™ and AYGESTIN™ (norethindrone acetate); progesterone implants such as NORPLANT SYSTEM™ (subdermal implants of norgestrel); antiprogestins such as RU 486™ (mifepristone); hormonal contraceptives such as ENOVID™ (norethynodrel plus mestranol), PROGESTASERT™ (intrauterine device that releases progesterone), LOESTRIN™, BREVICON™, MODICON™, GENORA™, NELONA™, NORINYL™, OVACON-35™ and OVACON-50™ (ethinyl estradiol/norethindrone), LEVLEN™, NORDETTE™, TRI-LEVLEN™ and TRIPHASIL-21 ™ (ethinyl estradiol/levonorgestrel) LO/OVRAL™ and OVRAL™ (ethinyl estradiol/norgestrel), DEMULEN™ (ethinyl estradiol/ethynodiol diacetate), NORINYL™, ORTHO-NOVUM™, NORETHIN™, GENORA™, and NELOVA™ (norethindrone/mestranol), DESOGEN™ and ORTHO-CEPT™ (ethinyl estradiol/desogestrel), ORTHO-CYCLEN™ and ORTHO-TRICYCLEN™ (ethinyl estradiol/norgestimate), MICRONOR™ and NOR-QD™ (norethindrone), and OVRETTE™ (norgestrel).

Additional treatments for endocrine and/or hormone imbalance disorders include, but are not limited to, testosterone esters such as methenolone acetate and testosterone undecanoate; parenteral and oral androgens such as TESTOJECT-50™ (testosterone), TESTEX™ (testosterone propionate), DELATESTRYL™ (testosterone enanthate), DEPO-TESTOSTERONE™ (testosterone cypionate), DANOCRINE™ (danazol), HALOTESTIN™ (fluoxymesterone), ORETON METHYL™, TESTRED™ and VIRILON™ (methyltestosterone), and OXANDRIN™ (oxandrolone); testosterone transdermal systems such as TESTODERM™; androgen receptor antagonist and 5-alpha-reductase inhibitors such as ANDROCUR™ (cyproterone acetate), EULEXIN™ (flutamide), and PROSCAR™ (finasteride); adrenocorticotropic hormone preparations such as CORTROSYN™ (cosyntropin); adrenocortical steroids and their synthetic analogs such as ACLOVATE™ (alclometasone dipropionate), CYCLOCORT™ (amcinonide), BECLOVENT™ and VANCERIL™ (beclomethasone dipropionate), CELESTONE™ (betamethasone), BENISONE™ and UTICORT™ (betamethasone benzoate), DIPROSONE™ (betamethasone dipropionate), CELESTONE PHOSPHATE™ (betamethasone sodium phosphate), CELESTONE SOLUSPAN™ (betamethasone sodium phosphate and acetate), BETA-VAL™ and VALISONE™ (betamethasone valerate), TEMOVATE™ (clobetasol propionate), CLODERM™ (clocortolone pivalate), CORTEF™ and HYDROCORTONE™ (cortisol (hydrocortisone)), HYDROCORTONE ACETATE™ (cortisol (hydrocortisone) acetate), LOCOID™ (cortisol (hydrocortisone) butyrate), HYDROCORTONE PHOSPHATE™ (cortisol (hydrocortisone) sodium phosphate), A-HYDROCORT™ and SOLU CORTEF™ (cortisol (hydrocortisone) sodium succinate), WESTCORT™ (cortisol (hydrocortisone) valerate), CORTISONE ACETATE™ (cortisone acetate), DESOWEN™ and TRIDESILON™ (desonide), TOPICORT™ (desoximetasone), DECADRON™ (dexamethasone), DECADRON LA™ (dexamethasone acetate), DECADRON PHOSPHATE™ and HEXADROL PHOSPHATE™ (dexamethasone sodium phosphate), FLORONE™ and MAXIFLOR™ (diflorasone diacetate), FLORINEF ACETATE™ (fludrocortisone acetate), AEROBID™ and NASALIDE™ (flunisolide), FLUONID™ and SYNALAR™ (fluocinolone acetonide), LIDEX™ (fluocinonide), FLUOR-OP™ and FML™ (fluorometholone), CORDRAN™ (flurandrenolide), HALOG™ (halcinonide), HMS LIZUIFILM™ (medrysone), MEDROL™ (methylprednisolone), DEPO-MEDROL™ and MEDROL ACETATE™ (methylprednisone acetate), A-METHAPRED™ and SOLUMEDROL™ (methylprednisolone sodium succinate), ELOCON™ (mometasone furoate), HALDRONE™ (paramethasone acetate), DELTA-CORTEF™ (prednisolone), ECONOPRED™ (prednisolone acetate), HYDELTRASOL™ (prednisolone sodium phosphate), HYDELTRA-T.B.A™ (prednisolone tebutate), DELTASONE™ (prednisone), ARISTOCORT™ and KENACORT™ (triamcinolone), KENALOG™ (triamcinolone acetonide), ARISTOCORT™ and KENACORT DIACETATE™ (triamcinolone diacetate), and ARISTOSPAN™ (triamcinolone hexacetonide); inhibitors of biosynthesis and action of adrenocortical steroids such as CYTADREN™ (aminoglutethimide), NIZORAL™ (ketoconazole), MODRASTANE™ (trilostane), and METOPIRONE™ (metyrapone); bovine, porcine or human insulin or mixtures thereof, insulin analogs; recombinant human insulin such as HUMULIN™ and NOVOLIN™; oral hypoglycemic agents such as ORAMIDE™ and ORINASE™ (tolbutamide), DIABINESE™ (chlorpropamide), TOLAMIDE™ and TOLINASE™ (tolazamide), DYMELOR™ (acetohexamide), glibenclamide, MICRONASE™, DIBETA™ and GLYNASE™ (glyburide), GLUCOTROL™ (glipizide), and DIAMICRON™ (gliclazide), GLUCOPHAGE™ (metformin), ciglitazone, pioglitazone, and alpha-glucosidase inhibitors; bovine or porcine glucagon; somatostatins such as SANDOSTATIN™ (octreotide); and diazoxides such as PROGLYCEM™ (diazoxide).

In one embodiment, the Therapeutics of the invention are administered in combination with treatments for uterine motility disorders. Treatments for uterine motility disorders include, but are not limited to, estrogen drugs such as conjugated estrogens (e.g., PREMARIN® and ESTRATAB®), estradiols (e.g., CLIMARA® and ALORA®), estropipate, and chlorotrianisene; progestin drugs (e.g., AMEN® (medroxyprogesterone), MICRONOR® (norethidrone acetate), PROMETRIUM® progesterone, and megestrol acetate); and estrogen/progesterone combination therapies such as, for example, conjugated estrogens/medroxyprogesterone (e.g., PREMPRO™ and PREMPHASE®) and norethindrone acetate/ethinyl estsradiol (e.g., FEMHRT™).

In an additional embodiment, the Therapeutics of the invention are administered in combination with drugs effective in treating iron deficiency and hypochromic anemias, including but not limited to, ferrous sulfate (iron sulfate, FEOSOL™), ferrous fumarate (e.g., FEOSTAT™), ferrous gluconate (e.g., FERGON™), polysaccharide-iron complex (e.g., NIFEREX™), iron dextran injection (e.g., INFED™), cupric sulfate, pyroxidine, riboflavin, Vitamin B₁₂, cyancobalamin injection (e.g., REDISOL™, RUBRAMIN PC™), hydroxocobalamin, folic acid (e.g., FOLVITE™), leucovorin (folinic acid, 5-CHOH4PteGlu, citrovorum factor) or WELLCOVORIN (Calcium salt of leucovorin), transferrin or ferritin.

In certain embodiments, the Therapeutics of the invention are administered in combination with agents used to treat psychiatric disorders. Psychiatric drugs that may be administered with the Therapeutics of the invention include, but are not limited to, antipsychotic agents (e.g., chlorpromazine, chlorprothixene, clozapine, fluphenazine, haloperidol, loxapine, mesoridazine, molindone, olanzapine, perphenazine, pimozide, quetiapine, risperidone, thioridazine, thiothixene, trifluoperazine, and triflupromazine), antimanic agents (e.g., carbamazepine, divalproex sodium, lithium carbonate, and lithium citrate), antidepressants (e.g., amitriptyline, amoxapine, bupropion, citalopram, clomipramine, desipramine, doxepin, fluvoxamine, fluoxetine, imipramine, isocarboxazid, maprotiline, mirtazapine, nefazodone, nortriptyline, paroxetine, phenelzine, protriptyline, sertraline, tranylcypromine, trazodone, trimipramine, and venlafaxine), antianxiety agents (e.g., alprazolam, buspirone, chlordiazepoxide, clorazepate, diazepam, halazepam, lorazepam, oxazepam, and prazepam), and stimulants (e.g., d-amphetamine, methylphenidate, and pemoline).

In other embodiments, the Therapeutics of the invention are administered in combination with agents used to treat neurological disorders. Neurological agents that may be administered with the Therapeutics of the invention include, but are not limited to, antiepileptic agents (e.g., carbamazepine, clonazepam, ethosuximide, phenobarbital, phenyloin, primidone, valproic acid, divalproex sodium, felbamate, gabapentin, lamotrigine, levetiracetam, oxcarbazepine, tiagabine, topiramate, zonisamide, diazepam, lorazepam, and clonazepam), antiparkinsonian agents (e.g., levodopa/carbidopa, selegiline, amantidine, bromocriptine, pergolide, ropinirole, pramipexole, benztropine; biperiden; ethopropazine; procyclidine; trihexyphenidyl, tolcapone), and ALS therapeutics (e.g. riluzole).

In another embodiment, Therapeutics of the invention are administered in combination with vasodilating agents and/or calcium channel blocking agents. Vasodilating agents that may be administered with the Therapeutics of the invention include, but are not limited to, Angiotensin Converting Enzyme (ACE) inhibitors (e.g., papaverine, isoxsuprine, benazepril, captopril, cilazapril, enalapril, enalaprilat, fosinopril, lisinopril, moexipril, perindopril, quinapril, ramipril, spirapril, trandolapril, and nylidrin), and nitrates (e.g., isosorbide dinitrate, isosorbide mononitrate, and nitroglycerin). Examples of calcium channel blocking agents that may be administered in combination with the Therapeutics of the invention include, but are not limited to amlodipine, bepridil, diltiazem, felodipine, flunarizine, isradipine, nicardipine, nifedipine, nimodipine, and verapamil.

In certain embodiments, the Therapeutics of the invention are administered in combination with treatments for gastrointestinal disorders. Treatments for gastrointestinal disorders that may be administered with the Therapeutic of the invention include, but are not limited to, H₂ histamine receptor antagonists (e.g., TAGAMET™ (cimetidine), ZANTAC™ (ranitidine), PEPCID™ (famotidine), and AXID™ (nizatidine)); inhibitors of H⁺, K⁺ ATPase (e.g., PREVACID™ (lansoprazole) and PRILOSEC™ (omeprazole)); Bismuth compounds (e.g., PEPTO-BISMOL™ (bismuth subsalicylate) and DE-NOL™ (bismuth subcitrate)); various antacids; sucralfate; prostaglandin analogs (e.g. CYTOTEC™ (misoprostol)); muscarinic cholinergic antagonists; laxatives (e.g., surfactant laxatives, stimulant laxatives, saline and osmotic laxatives); antidiarrheal agents (e.g., LOMOTIL™ (diphenoxylate), MOTOFEN™ (diphenoxin), and IMODIUM™ (loperamide hydrochloride)), synthetic analogs of somatostatin such as SANDOSTATIN™ (octreotide), antiemetic agents (e.g., ZOFRAN™ (ondansetron), KYTRIL™ (granisetron hydrochloride), tropisetron, dolasetron, metoclopramide, chlorpromazine, perphenazine, prochlorperazine, promethazine, thiethylperazine, triflupromazine, domperidone, haloperidol, droperidol, trimethobenzamide, dexamethasone, methylprednisolone, dronabinol, and nabilone); D2 antagonists (e.g., metoclopramide, trimethobenzamide and chlorpromazine); bile salts; chenodeoxycholic acid; ursodeoxycholic acid; and pancreatic enzyme preparations such as pancreatin and pancrelipase.

In additional embodiments, the Therapeutics of the invention are administered in combination with other therapeutic or prophylactic regimens, such as, for example, radiation therapy.

Example 14 Method of Treating Decreased Levels of the Polypeptide

The present invention relates to a method for treating an individual in need of an increased level of a polypeptide of the invention in the body comprising administering to such an individual a composition comprising a therapeutically effective amount of polypeptides (including agonists thereto), and/or antibodies of the invention. Moreover, it will be appreciated that conditions caused by a decrease in the standard or normal expression level of a polypeptide of the present invention in an individual may be treated by administering agonists of said polypeptide. Thus, the invention also provides a method of treatment of an individual in need of an increased level of the polypeptide comprising administering to such an individual a Therapeutic comprising an amount of the agonist (including polypeptides and antibodies of the present invention) to increase the activity level of the polypeptide in such an individual.

For example, a patient with decreased levels of a polypeptide receives a daily dose 0.1-100 ug/kg of the agonist for six consecutive days. The exact details of the dosing scheme, based on administration and formulation, are provided in Example 13.

Example 15 Method of Treating Increased Levels of the Polypeptide

The present invention also relates to a method of treating an individual in need of a decreased level of a polypeptide of the invention in the body comprising administering to such an individual a composition comprising a therapeutically effective amount of an antagonist of the invention (including polypeptides and antibodies of the invention).

In one example, antisense technology is used to inhibit production of a polypeptide of the present invention. This technology is one example of a method of decreasing levels of a polypeptide, due to a variety of etiologies, such as cancer.

For example, a patient diagnosed with abnormally increased levels of a polypeptide is administered intravenously antisense polynucleotides at 0.5, 1.0, 1.5, 2.0 and 3.0 mg/kg day for 21 days. This treatment is repeated after a 7-day rest period if the treatment was well tolerated. The antisense polynucleotides of the present invention can be formulated using techniques and formulations described herein (e.g. see Example 13), or otherwise known in the art.

Example 16 Method of Treatment Using Gene Therapy-Ex Vivo

One method of gene therapy transplants fibroblasts, which are capable of expressing a polypeptide, onto a patient. Generally, fibroblasts are obtained from a subject by skin biopsy. The resulting tissue is placed in tissue-culture medium and separated into small pieces. Small chunks of the tissue are placed on a wet surface of a tissue culture flask, approximately ten pieces are placed in each flask. The flask is turned upside down, closed tight and left at room temperature over night. After 24 hours at room temperature, the flask is inverted and the chunks of tissue remain fixed to the bottom of the flask and fresh media (e.g., Ham's F12 media, with 10% FBS, penicillin and streptomycin) is added. The flasks are then incubated at 37 degree C. for approximately one week.

At this time, fresh media is added and subsequently changed every several days. After an additional two weeks in culture, a monolayer of fibroblasts emerge. The monolayer is trypsinized and scaled into larger flasks.

pMV-7 (Kirschmeier, P. T. et al., DNA, 7:219-25 (1988)), flanked by the long terminal repeats of the Moloney murine sarcoma virus, is digested with EcoRI and HindIII and subsequently treated with calf intestinal phosphatase. The linear vector is fractionated on agarose gel and purified, using glass beads.

The cDNA encoding a polypeptide of the present invention can be amplified using PCR primers which correspond to the 5′ and 3′ end sequences respectively as set forth in Example 1 using primers and having appropriate restriction sites and initiation/stop codons, if necessary. Preferably, the 5′ primer contains an EcoRI site and the 3′ primer includes a HindIII site. Equal quantities of the Moloney murine sarcoma virus linear backbone and the amplified EcoRI and HindIII fragment are added together, in the presence of T4 DNA ligase. The resulting mixture is maintained under conditions appropriate for ligation of the two fragments. The ligation mixture is then used to transform bacteria HB101, which are then plated onto agar containing kanamycin for the purpose of confirming that the vector has the gene of interest properly inserted.

The amphotropic pA317 or GP+am12 packaging cells are grown in tissue culture to confluent density in Dulbecco's Modified Eagles Medium (DMEM) with 10% calf serum (CS), penicillin and streptomycin. The MSV vector containing the gene is then added to the media and the packaging cells transduced with the vector. The packaging cells now produce infectious viral particles containing the gene (the packaging cells are now referred to as producer cells).

Fresh media is added to the transduced producer cells, and subsequently, the media is harvested from a 10 cm plate of confluent producer cells. The spent media, containing the infectious viral particles, is filtered through a millipore filter to remove detached producer cells and this media is then used to infect fibroblast cells. Media is removed from a sub-confluent plate of fibroblasts and quickly replaced with the media from the producer cells. This media is removed and replaced with fresh media. If the titer of virus is high, then virtually all fibroblasts will be infected and no selection is required. If the titer is very low, then it is necessary to use a retroviral vector that has a selectable marker, such as neo or his. Once the fibroblasts have been efficiently infected, the fibroblasts are analyzed to determine whether protein is produced.

The engineered fibroblasts are then transplanted onto the host, either alone or after having been grown to confluence on cytodex 3 microcarrier beads.

Example 17 Gene Therapy Using Endogenous Genes Corresponding to Polynucleotides of the Invention

Another method of gene therapy according to the present invention involves operably associating the endogenous polynucleotide sequence of the invention with a promoter via homologous recombination as described, for example, in U.S. Pat. No. 5,641,670, issued Jun. 24, 1997; International Publication NO: WO 96/29411, published Sep. 26, 1996; International Publication NO: WO 94/12650, published Aug. 4, 1994; Koller et al., Proc. Natl. Acad. Sci. USA, 86:8932-8935 (1989); and Zijlstra et al., Nature, 342:435-438 (1989). This method involves the activation of a gene which is present in the target cells, but which is not expressed in the cells, or is expressed at a lower level than desired.

Polynucleotide constructs are made which contain a promoter and targeting sequences, which are homologous to the 5′ non-coding sequence of endogenous polynucleotide sequence, flanking the promoter. The targeting sequence will be sufficiently near the 5′ end of the polynucleotide sequence so the promoter will be operably linked to the endogenous sequence upon homologous recombination. The promoter and the targeting sequences can be amplified using PCR. Preferably, the amplified promoter contains distinct restriction enzyme sites on the 5′ and 3′ ends. Preferably, the 3′ end of the first targeting sequence contains the same restriction enzyme site as the 5′ end of the amplified promoter and the 5′ end of the second targeting sequence contains the same restriction site as the 3′ end of the amplified promoter.

The amplified promoter and the amplified targeting sequences are digested with the appropriate restriction enzymes and subsequently treated with calf intestinal phosphatase. The digested promoter and digested targeting sequences are added together in the presence of T4 DNA ligase. The resulting mixture is maintained under conditions appropriate for ligation of the two fragments. The construct is size fractionated on an agarose gel, then purified by phenol extraction and ethanol precipitation.

In this Example, the polynucleotide constructs are administered as naked polynucleotides via electroporation. However, the polynucleotide constructs may also be administered with transfection-facilitating agents, such as liposomes, viral sequences, viral particles, precipitating agents, etc. Such methods of delivery are known in the art.

Once the cells are transfected, homologous recombination will take place which results in the promoter being operably linked to the endogenous polynucleotide sequence. This results in the expression of polynucleotide corresponding to the polynucleotide in the cell. Expression may be detected by immunological staining, or any other method known in the art.

Fibroblasts are obtained from a subject by skin biopsy. The resulting tissue is placed in DMEM+10% fetal calf serum. Exponentially growing or early stationary phase fibroblasts are trypsinized and rinsed from the plastic surface with nutrient medium. An aliquot of the cell suspension is removed for counting, and the remaining cells are subjected to centrifugation. The supernatant is aspirated and the pellet is resuspended in 5 ml of electroporation buffer (20 mM HEPES pH 7.3, 137 mM NaCl, 5 mM KCl, 0.7 mM Na₂ HPO₄, 6 mM dextrose). The cells are recentrifuged, the supernatant aspirated, and the cells resuspended in electroporation buffer containing 1 mg/ml acetylated bovine serum albumin. The final cell suspension contains approximately 3×10⁶ cells/ml. Electroporation should be performed immediately following resuspension.

Plasmid DNA is prepared according to standard techniques. For example, to construct a plasmid for targeting to the locus corresponding to the polynucleotide of the invention, plasmid pUC18 (MBI Fermentas, Amherst, N.Y.) is digested with HindIII. The CMV promoter is amplified by PCR with an XbaI site on the 5′ end and a BamHI site on the 3′ end. Two non-coding sequences are amplified via PCR: one non-coding sequence (fragment 1) is amplified with a HindIII site at the 5′ end and an Xba site at the 3′ end; the other non-coding sequence (fragment 2) is amplified with a BamHI site at the 5′ end and a HindIII site at the 3′ end. The CMV promoter and the fragments (1 and 2) are digested with the appropriate enzymes (CMV promoter—XbaI and BamHI; fragment 1—XbaI; fragment 2—BamHI) and ligated together. The resulting ligation product is digested with HindIII, and ligated with the HindIII-digested pUC18 plasmid.

Plasmid DNA is added to a sterile cuvette with a 0.4 cm electrode gap (Bio-Rad). The final DNA concentration is generally at least 120 μg/ml. 0.5 ml of the cell suspension (containing approximately 1.5.×10⁶ cells) is then added to the cuvette, and the cell suspension and DNA solutions are gently mixed. Electroporation is performed with a Gene-Pulser apparatus (Bio-Rad). Capacitance and voltage are set at 960 μF and 250-300 V, respectively. As voltage increases, cell survival decreases, but the percentage of surviving cells that stably incorporate the introduced DNA into their genome increases dramatically. Given these parameters, a pulse time of approximately 14-20 mSec should be observed.

Electroporated cells are maintained at room temperature for approximately 5 min, and the contents of the cuvette are then gently removed with a sterile transfer pipette. The cells are added directly to 10 ml of prewarmed nutrient media (DMEM with 15% calf serum) in a 10 cm dish and incubated at 37 degree C. The following day, the media is aspirated and replaced with 10 ml of fresh media and incubated for a further 16-24 hours.

The engineered fibroblasts are then injected into the host, either alone or after having been grown to confluence on cytodex 3 microcarrier beads. The fibroblasts now produce the protein product. The fibroblasts can then be introduced into a patient as described above.

Example 18 Method of Treatment Using Gene Therapy—In Vivo

Another aspect of the present invention is using in vivo gene therapy methods to prevent, treat, and/or ameliorate cancer or other hyperproliferative diseases and disorders. The gene therapy method relates to the introduction of naked nucleic acid (DNA, RNA, and antisense DNA or RNA) sequences into an animal to increase or decrease the expression of the polypeptide. The polynucleotide of the present invention may be operatively linked to (i.e., associated with) a promoter or any other genetic elements necessary for the expression of the polypeptide by the target tissue. Such gene therapy and delivery techniques and methods are known in the art, see, for example, WO90/11092, WO98/11779; U.S. Pat. Nos. 5,693,622, 5,705,151, 5,580,859; Tabata et al., Cardiovasc. Res. 35(3):470-479 (1997); Chao et al., Pharmacol. Res. 35(6):517-522 (1997); Wolff, Neuromuscul. Disord. 7(5):314-318 (1997); Schwartz et al., Gene Ther. 3(5):405-411 (1996); Tsurumi et al., Circulation 94(12):3281-3290 (1996) (incorporated herein by reference).

The polynucleotide constructs may be delivered by any method that delivers injectable materials to the cells of an animal, such as, injection into the interstitial space of tissues (heart, muscle, skin, lung, liver, intestine and the like). The polynucleotide constructs can be delivered in a pharmaceutically acceptable liquid or aqueous carrier.

The term “naked” polynucleotide, DNA or RNA, refers to sequences that are free from any delivery vehicle that acts to assist, promote, or facilitate entry into the cell, including viral sequences, viral particles, liposome formulations, LIPOFECTIN™ or precipitating agents and the like. However, the polynucleotides of the present invention may also be delivered in liposome formulations (such as those taught in Felgner P. L. et al. (1995) Ann. NY Acad. Sci. 772:126-139 and Abdallah B. et al. (1995) Biol. Cell 85(1): 1-7) which can be prepared by methods well known to those skilled in the art.

The polynucleotide vector constructs used in the gene therapy method are preferably constructs that will not integrate into the host genome nor will they contain sequences that allow for replication. Any strong promoter known to those skilled in the art can be used for driving the expression of DNA. Unlike other gene therapy techniques, one major advantage of introducing naked nucleic acid sequences into target cells is the transitory nature of the polynucleotide synthesis in the cells. Studies have shown that non-replicating DNA sequences can be introduced into cells to provide production of the desired polypeptide for periods of up to six months.

The polynucleotide construct can be delivered to the interstitial space of tissues within an animal, including muscle, skin, brain, lung, liver, spleen, bone marrow, thymus, heart, lymph, blood, bone, cartilage, pancreas, kidney, gall bladder, stomach, intestine, testis, ovary, uterus, rectum, nervous system, eye, gland, and connective tissue. Interstitial space of the tissues comprises the intercellular fluid, mucopolysaccharide matrix among the reticular fibers of organ tissues, elastic fibers in the walls of vessels or chambers, collagen fibers of fibrous tissues, or that same matrix within connective tissue ensheathing muscle cells or in the lacunae of bone. It is similarly the space occupied by the plasma of the circulation and the lymph fluid of the lymphatic channels. Delivery to the interstitial space of muscle tissue is preferred for the reasons discussed below. They may be conveniently delivered by injection into the tissues comprising these cells. They are preferably delivered to and expressed in persistent, non-dividing cells which are differentiated, although delivery and expression may be achieved in non-differentiated or less completely differentiated cells, such as, for example, stem cells of blood or skin fibroblasts. In vivo muscle cells are particularly competent in their ability to take up and express polynucleotides.

For the naked polynucleotide injection, an effective dosage amount of DNA or RNA will be in the range of from about 0.05 g/kg body weight to about 50 mg/kg body weight. Preferably the dosage will be from about 0.005 mg/kg to about 20 mg/kg and more preferably from about 0.05 mg/kg to about 5 mg/kg. Of course, as the artisan of ordinary skill will appreciate, this dosage will vary according to the tissue site of injection. The appropriate and effective dosage of nucleic acid sequence can readily be determined by those of ordinary skill in the art and may depend on the condition being treated and the route of administration. The preferred route of administration is by the parenteral route of injection into the interstitial space of tissues. However, other parenteral routes may also be used, such as, inhalation of an aerosol formulation particularly for delivery to lungs or bronchial tissues, throat or mucous membranes of the nose. In addition, naked polynucleotide constructs can be delivered to arteries during angioplasty by the catheter used in the procedure.

The dose response effects of injected polynucleotide in muscle in vivo is determined as follows. Suitable template DNA for production of mRNA coding for polypeptide of the present invention is prepared in accordance with a standard recombinant DNA methodology. The template DNA, which may be either circular or linear, is either used as naked DNA or complexed with liposomes. The quadriceps muscles of mice are then injected with various amounts of the template DNA.

Five to six week old female and male Balb/C mice are anesthetized by intraperitoneal injection with 0.3 ml of 2.5% Avertin. A 1.5 cm incision is made on the anterior thigh, and the quadriceps muscle is directly visualized. The template DNA is injected in 0.1 ml of carrier in a 1 cc syringe through a 27 gauge needle over one minute, approximately 0.5 cm from the distal insertion site of the muscle into the knee and about 0.2 cm deep. A suture is placed over the injection site for future localization, and the skin is closed with stainless steel clips.

After an appropriate incubation time (e.g., 7 days) muscle extracts are prepared by excising the entire quadriceps. Every fifth 15 um cross-section of the individual quadriceps muscles is histochemically stained for protein expression. A time course for protein expression may be done in a similar fashion except that quadriceps from different mice are harvested at different times. Persistence of DNA in muscle following injection may be determined by Southern blot analysis after preparing total cellular DNA and HIRT supernatants from injected and control mice. The results of the above experimentation in mice can be used to extrapolate proper dosages and other treatment parameters in humans and other animals using naked DNA.

Example 19 Transgenic Animals

The polypeptides of the invention can also be expressed in transgenic animals. Animals of any species, including, but not limited to, mice, rats, rabbits, hamsters, guinea pigs, pigs, micro-pigs, goats, sheep, cows and non-human primates, e.g., baboons, monkeys, and chimpanzees may be used to generate transgenic animals. In a specific embodiment, techniques described herein or otherwise known in the art, are used to express polypeptides of the invention in humans, as part of a gene therapy protocol.

Any technique known in the art may be used to introduce the transgene (i.e., polynucleotides of the invention) into animals to produce the founder lines of transgenic animals. Such techniques include, but are not limited to, pronuclear microinjection (Paterson et al., Appl. Microbiol. Biotechnol. 40:691-698 (1994); Carver et al., Biotechnology (NY) 11:1263-1270 (1993); Wright et al., Biotechnology (NY) 9:830-834 (1991); and Hoppe et al., U.S. Pat. No. 4,873,191 (1989)); retrovirus mediated gene transfer into germ lines (Van der Putten et al., Proc. Natl. Acad. Sci., USA 82:6148-6152 (1985)), blastocysts or embryos; gene targeting in embryonic stem cells (Thompson et al., Cell 56:313-321 (1989)); electroporation of cells or embryos (Lo, 1983, Mol. Cell. Biol. 3:1803-1814 (1983)); introduction of the polynucleotides of the invention using a gene gun (see, e.g., Ulmer et al., Science 259:1745 (1993); introducing nucleic acid constructs into embryonic pleuripotent stem cells and transferring the stem cells back into the blastocyst; and sperm-mediated gene transfer (Lavitrano et al., Cell 57:717-723 (1989); etc. For a review of such techniques, see Gordon, “Transgenic Animals,” Intl. Rev. Cytol. 115:171-229 (1989), which is incorporated by reference herein in its entirety.

Any technique known in the art may be used to produce transgenic clones containing polynucleotides of the invention, for example, nuclear transfer into enucleated oocytes of nuclei from cultured embryonic, fetal, or adult cells induced to quiescence (Campell et al., Nature 380:64-66 (1996); Wilmut et al., Nature 385:810-813 (1997)).

The present invention provides for transgenic animals that carry the transgene in all their cells, as well as animals which carry the transgene in some, but not all their cells, i.e., mosaic animals or chimeric. The transgene may be integrated as a single transgene or as multiple copies such as in concatamers, e.g., head-to-head tandems or head-to-tail tandems. The transgene may also be selectively introduced into and activated in a particular cell type by following, for example, the teaching of Lasko et al. (Lasko et al., Proc. Natl. Acad. Sci. USA 89:6232-6236 (1992)). The regulatory sequences required for such a cell-type specific activation will depend upon the particular cell type of interest, and will be apparent to those of skill in the art. When it is desired that the polynucleotide transgene be integrated into the chromosomal site of the endogenous gene, gene targeting is preferred. Briefly, when such a technique is to be utilized, vectors containing some nucleotide sequences homologous to the endogenous gene are designed for the purpose of integrating, via homologous recombination with chromosomal sequences, into and disrupting the function of the nucleotide sequence of the endogenous gene. The transgene may also be selectively introduced into a particular cell type, thus inactivating the endogenous gene in only that cell type, by following, for example, the teaching of Gu et al. (Gu et al., Science 265:103-106 (1994)). The regulatory sequences required for such a cell-type specific inactivation will depend upon the particular cell type of interest, and will be apparent to those of skill in the art.

Once transgenic animals have been generated, the expression of the recombinant gene may be assayed utilizing standard techniques. Initial screening may be accomplished by Southern blot analysis or PCR techniques to analyze animal tissues to verify that integration of the transgene has taken place. The level of mRNA expression of the transgene in the tissues of the transgenic animals may also be assessed using techniques which include, but are not limited to, Northern blot analysis of tissue samples obtained from the animal, in situ hybridization analysis, and reverse transcriptase-PCR (rt-PCR). Samples of transgenic gene-expressing tissue may also be evaluated immunocytochemically or immunohistochemically using antibodies specific for the transgene product.

Once the founder animals are produced, they may be bred, inbred, outbred, or crossbred to produce colonies of the particular animal. Examples of such breeding strategies include, but are not limited to: outbreeding of founder animals with more than one integration site in order to establish separate lines; inbreeding of separate lines in order to produce compound transgenics that express the transgene at higher levels because of the effects of additive expression of each transgene; crossing of heterozygous transgenic animals to produce animals homozygous for a given integration site in order to both augment expression and eliminate the need for screening of animals by DNA analysis; crossing of separate homozygous lines to produce compound heterozygous or homozygous lines; and breeding to place the transgene on a distinct background that is appropriate for an experimental model of interest.

Transgenic animals of the invention have uses which include, but are not limited to, animal model systems useful in elaborating the biological function of polypeptides of the present invention, studying conditions and/or disorders associated with aberrant expression, and in screening for compounds effective in ameliorating such conditions and/or disorders.

Example 20 Knock-Out Animals

Endogenous gene expression can also be reduced by inactivating or “knocking out” the gene and/or its promoter using targeted homologous recombination. (e.g., see Smithies et al., Nature 317:230-234 (1985); Thomas & Capecchi, Cell 51:503-512 (1987); Thompson et al., Cell 5:313-321 (1989); each of which is incorporated by reference herein in its entirety). For example, a mutant, non-functional polynucleotide of the invention (or a completely unrelated DNA sequence) flanked by DNA homologous to the endogenous polynucleotide sequence (either the coding regions or regulatory regions of the gene) can be used, with or without a selectable marker and/or a negative selectable marker, to transfect cells that express polypeptides of the invention in vivo. In another embodiment, techniques known in the art are used to generate knockouts in cells that contain, but do not express the gene of interest. Insertion of the DNA construct, via targeted homologous recombination, results in inactivation of the targeted gene. Such approaches are particularly suited in research and agricultural fields where modifications to embryonic stem cells can be used to generate animal offspring with an inactive targeted gene (e.g., see Thomas & Capecchi 1987 and Thompson 1989, supra). However this approach can be routinely adapted for use in humans provided the recombinant DNA constructs are directly administered or targeted to the required site in vivo using appropriate viral vectors that will be apparent to those of skill in the art.

In further embodiments of the invention, cells that are genetically engineered to express the polypeptides of the invention, or alternatively, that are genetically engineered not to express the polypeptides of the invention (e.g., knockouts) are administered to a patient in vivo. Such cells may be obtained from the patient (i.e., animal, including human) or an MHC compatible donor and can include, but are not limited to fibroblasts, bone marrow cells, blood cells (e.g., lymphocytes), adipocytes, muscle cells, endothelial cells etc. The cells are genetically engineered in vitro using recombinant DNA techniques to introduce the coding sequence of polypeptides of the invention into the cells, or alternatively, to disrupt the coding sequence and/or endogenous regulatory sequence associated with the polypeptides of the invention, e.g., by transduction (using viral vectors, and preferably vectors that integrate the transgene into the cell genome) or transfection procedures, including, but not limited to, the use of plasmids, cosmids, YACs, naked DNA, electroporation, liposomes, etc. The coding sequence of the polypeptides of the invention can be placed under the control of a strong constitutive or inducible promoter or promoter/enhancer to achieve expression, and preferably secretion, of the polypeptides of the invention. The engineered cells which express and preferably secrete the polypeptides of the invention can be introduced into the patient systemically, e.g., in the circulation, or intraperitoneally.

Alternatively, the cells can be incorporated into a matrix and implanted in the body, e.g., genetically engineered fibroblasts can be implanted as part of a skin graft; genetically engineered endothelial cells can be implanted as part of a lymphatic or vascular graft. (See, for example, Anderson et al. U.S. Pat. No. 5,399,349; and Mulligan & Wilson, U.S. Pat. No. 5,460,959 each of which is incorporated by reference herein in its entirety).

When the cells to be administered are non-autologous or non-MHC compatible cells, they can be administered using well known techniques which prevent the development of a host immune response against the introduced cells. For example, the cells may be introduced in an encapsulated form which, while allowing for an exchange of components with the immediate extracellular environment, does not allow the introduced cells to be recognized by the host immune system.

Transgenic and “knock-out” animals of the invention have uses which include, but are not limited to, animal model systems useful in elaborating the biological function of polypeptides of the present invention, studying conditions and/or disorders associated with aberrant expression, and in screening for compounds effective in ameliorating such conditions and/or disorders.

Example 21 Assays Detecting Stimulation or Inhibition of B Cell Proliferation and Differentiation

Generation of functional humoral immune responses requires both soluble and cognate signaling between B-lineage cells and their microenvironment. Signals may impart a positive stimulus that allows a B-lineage cell to continue its programmed development, or a negative stimulus that instructs the cell to arrest its current developmental pathway. To date, numerous stimulatory and inhibitory signals have been found to influence B cell responsiveness including IL-2, IL-4, IL-5, IL-6, IL-7, IL10, IL-13, IL-14 and IL-15. Interestingly, these signals are by themselves weak effectors but can, in combination with various co-stimulatory proteins, induce activation, proliferation, differentiation, homing, tolerance and death among B cell populations.

One of the best studied classes of B-cell co-stimulatory proteins is the TNF-superfamily. Within this family CD40, CD27, and CD30 along with their respective ligands CD154, CD70, and CD153 have been found to regulate a variety of immune responses. Assays which allow for the detection and/or observation of the proliferation and differentiation of these B-cell populations and their precursors are valuable tools in determining the effects various proteins may have on these B-cell populations in terms of proliferation and differentiation. Listed below are two assays designed to allow for the detection of the differentiation, proliferation, or inhibition of B-cell populations and their precursors.

In Vitro Assay—Agonists or antagonists of the invention can be assessed for its ability to induce activation, proliferation, differentiation or inhibition and/or death in B-cell populations and their precursors. The activity of the agonists or antagonists of the invention on purified human tonsillar B cells, measured qualitatively over the dose range from 0.1 to 10,000 ng/mL, is assessed in a standard B-lymphocyte co-stimulation assay in which purified tonsillar B cells are cultured in the presence of either formalin-fixed Staphylococcus aureus Cowan I (SAC) or immobilized anti-human IgM antibody as the priming agent. Second signals such as IL-2 and IL-15 synergize with SAC and IgM crosslinking to elicit B cell proliferation as measured by tritiated-thymidine incorporation. Novel synergizing agents can be readily identified using this assay. The assay involves isolating human tonsillar B cells by magnetic bead (MACS) depletion of CD3-positive cells. The resulting cell population is greater than 95% B cells as assessed by expression of CD45R(B220).

Various dilutions of each sample are placed into individual wells of a 96-well plate to which are added 10⁵ B-cells suspended in culture medium (RPMI 1640 containing 10% FBS, 5×10⁻⁵M 2ME, 100 U/ml penicillin, 10 ug/ml streptomycin, and 10⁻⁵ dilution of SAC) in a total volume of 150 ul. Proliferation or inhibition is quantitated by a 20 h pulse (1 uCi/well) with 3H-thymidine (6.7 Ci/mM) beginning 72 h post factor addition. The positive and negative controls are IL2 and medium respectively.

In vivo Assay—BALB/c mice are injected (i.p.) twice per day with buffer only, or 2 mg/Kg of agonists or antagonists of the invention, or truncated forms thereof. Mice receive this treatment for 4 consecutive days, at which time they are sacrificed and various tissues and serum collected for analyses. Comparison of H&E sections from normal spleens and spleens treated with agonists or antagonists of the invention identify the results of the activity of the agonists or antagonists on spleen cells, such as the diffusion of peri-arterial lymphatic sheaths, and/or significant increases in the nucleated cellularity of the red pulp regions, which may indicate the activation of the differentiation and proliferation of B-cell populations. Immunohistochemical studies using a B cell marker, anti-CD45R(B220), are used to determine whether any physiological changes to splenic cells, such as splenic disorganization, are due to increased B-cell representation within loosely defined B-cell zones that infiltrate established T-cell regions.

Flow cytometric analyses of the spleens from mice treated with agonist or antagonist is used to indicate whether the agonists or antagonists specifically increases the proportion of ThB+, CD45R(B220)dull B cells over that which is observed in control mice.

Likewise, a predicted consequence of increased mature B-cell representation in vivo is a relative increase in serum Ig titers. Accordingly, serum IgM and IgA levels are compared between buffer and agonists or antagonists-treated mice.

The studies described in this example tested activity of agonists or antagonists of the invention. However, one skilled in the art could easily modify the exemplified studies to test the activity of polynucleotides or polypeptides of the invention (e.g., gene therapy).

Example 22 T Cell Proliferation Assay

A CD3-induced proliferation assay is performed on PBMCs and is measured by the uptake of ³H-thymidine. The assay is performed as follows. Ninety-six well plates are coated with 100 μl/well of mAb to CD3 (HIT3a, Pharmingen) or isotype-matched control mAb (B33.1) overnight at 4 degrees C. (1 μg/ml in 0.05M bicarbonate buffer, pH 9.5), then washed three times with PBS. PBMC are isolated by F/H gradient centrifugation from human peripheral blood and added to quadruplicate wells (5×10⁴/well) of mAb coated plates in RPMI containing 10% FCS and P/S in the presence of varying concentrations of agonists or antagonists of the invention (total volume 200 ul). Relevant protein buffer and medium alone are controls. After 48 hr. culture at 37 degrees C., plates are spun for 2 min. at 1000 rpm and 100 μl of supernatant is removed and stored −20 degrees C. for measurement of IL-2 (or other cytokines) if effect on proliferation is observed. Wells are supplemented with 100 ul of medium containing 0.5 uCi of ³H-thymidine and cultured at 37 degrees C. for 18-24 hr. Wells are harvested and incorporation of ³H-thymidine used as a measure of proliferation. Anti-CD3 alone is the positive control for proliferation. IL-2 (100 U/ml) is also used as a control which enhances proliferation. Control antibody which does not induce proliferation of T cells is used as the negative control for the effects of agonists or antagonists of the invention.

The studies described in this example tested activity of agonists or antagonists of the invention. However, one skilled in the art could easily modify the exemplified studies to test the activity of polynucleotides or polypeptides of the invention (e.g., gene therapy).

Example 23 Effect of Agonists or Antagonists of the Invention on the Expression of MHC Class II, Costimulatory and Adhesion Molecules and Cell Differentiation of Monocytes and Monocyte-Derived Human Dendritic Cells

Dendritic cells are generated by the expansion of proliferating precursors found in the peripheral blood: adherent PBMC or elutriated monocytic fractions are cultured for 7-10 days with GM-CSF (50 ng/ml) and IL-4 (20 ng/ml). These dendritic cells have the characteristic phenotype of immature cells (expression of CD1, CD80, CD86, CD40 and MHC class II antigens). Treatment with activating factors, such as TNF-α, causes a rapid change in surface phenotype (increased expression of MHC class I and II, costimulatory and adhesion molecules, downregulation of FCγRII, upregulation of CD83). These changes correlate with increased antigen-presenting capacity and with functional maturation of the dendritic cells.

FACS analysis of surface antigens is performed as follows. Cells are treated 1-3 days with increasing concentrations of agonist or antagonist of the invention or LPS (positive control), washed with PBS containing 1% BSA and 0.02 mM sodium azide, and then incubated with 1:20 dilution of appropriate FITC- or PE-labeled monoclonal antibodies for 30 minutes at 4 degrees C. After an additional wash, the labeled cells are analyzed by flow cytometry on a FACScan (Becton Dickinson).

Effect on the production of cytokines. Cytokines generated by dendritic cells, in particular IL-12, are important in the initiation of T-cell dependent immune responses. IL-12 strongly influences the development of Th1 helper T-cell immune response, and induces cytotoxic T and NK cell function. An ELISA is used to measure the IL-12 release as follows. Dendritic cells (10⁶/ml) are treated with increasing concentrations of agonists or antagonists of the invention for 24 hours. LPS (100 ng/ml) is added to the cell culture as positive control. Supernatants from the cell cultures are then collected and analyzed for IL-12 content using commercial ELISA kit (e.g., R & D Systems (Minneapolis, Minn.)). The standard protocols provided with the kits are used.

Effect on the expression of MHC Class II, costimulatory and adhesion molecules. Three major families of cell surface antigens can be identified on monocytes: adhesion molecules, molecules involved in antigen presentation, and Fc receptor. Modulation of the expression of MHC class II antigens and other costimulatory molecules, such as B7 and ICAM-1, may result in changes in the antigen presenting capacity of monocytes and ability to induce T cell activation. Increased expression of Fc receptors may correlate with improved monocyte cytotoxic activity, cytokine release and phagocytosis.

FACS analysis is used to examine the surface antigens as follows. Monocytes are treated 1-5 days with increasing concentrations of agonists or antagonists of the invention or LPS (positive control), washed with PBS containing 1% BSA and 0.02 mM sodium azide, and then incubated with 1:20 dilution of appropriate FITC- or PE-labeled monoclonal antibodies for 30 minutes at 4 degrees C. After an additional wash, the labeled cells are analyzed by flow cytometry on a FACScan (Becton Dickinson).

Monocyte activation and/or increased survival. Assays for molecules that activate (or alternatively, inactivate) monocytes and/or increase monocyte survival (or alternatively, decrease monocyte survival) are known in the art and may routinely be applied to determine whether a molecule of the invention functions as an inhibitor or activator of monocytes. Agonists or antagonists of the invention can be screened using the three assays described below. For each of these assays, Peripheral blood mononuclear cells (PBMC) are purified from single donor leukopacks (American Red Cross, Baltimore, Md.) by centrifugation through a HISTOPAGUE™ gradient (SIGMA™). Monocytes are isolated from PBMC by counterflow centrifugal elutriation.

Monocyte Survival Assay. Human peripheral blood monocytes progressively lose viability when cultured in absence of serum or other stimuli. Their death results from internally regulated processes (apoptosis). Addition to the culture of activating factors, such as TNF-alpha dramatically improves cell survival and prevents DNA fragmentation. Propidium iodide (PI) staining is used to measure apoptosis as follows. Monocytes are cultured for 48 hours in polypropylene tubes in serum-free medium (positive control), in the presence of 100 ng/ml TNF-alpha (negative control), and in the presence of varying concentrations of the compound to be tested. Cells are suspended at a concentration of 2×10⁶/ml in PBS containing PI at a final concentration of 5 μg/ml, and then incubated at room temperature for 5 minutes before FACScan analysis. PI uptake has been demonstrated to correlate with DNA fragmentation in this experimental paradigm.

Effect on cytokine release. An important function of monocytes/macrophages is their regulatory activity on other cellular populations of the immune system through the release of cytokines after stimulation. An ELISA to measure cytokine release is performed as follows. Human monocytes are incubated at a density of 5×10⁵ cells/ml with increasing concentrations of agonists or antagonists of the invention and under the same conditions, but in the absence of agonists or antagonists. For IL-12 production, the cells are primed overnight with IFN (100 U/ml) in the presence of agonist or antagonist of the invention. LPS (10 ng/ml) is then added. Conditioned media are collected after 24 h and kept frozen until use. Measurement of TNF-alpha, IL-10, MCP-1 and IL-8 is then performed using a commercially available ELISA kit (e.g., R & D Systems (Minneapolis, Minn.)) and applying the standard protocols provided with the kit.

Oxidative burst. Purified monocytes are plated in 96-w plate at 2-1×10⁵ cell/well. Increasing concentrations of agonists or antagonists of the invention are added to the wells in a total volume of 0.2 ml culture medium (RPMI 1640+10% FCS, glutamine and antibiotics). After 3 days incubation, the plates are centrifuged and the medium is removed from the wells. To the macrophage monolayers, 0.2 ml per well of phenol red solution (140 mM NaCl, 10 mM potassium phosphate buffer pH 7.0, 5.5 mM dextrose, 0.56 mM phenol red and 19 U/ml of HRPO) is added, together with the stimulant (200 nM PMA). The plates are incubated at 37° C. for 2 hours and the reaction is stopped by adding 20 μl 1N NaOH per well. The absorbance is read at 610 nm. To calculate the amount of H₂O₂ produced by the macrophages, a standard curve of a H₂O₂ solution of known molarity is performed for each experiment.

The studies described in this example tested activity of agonists or antagonists of the invention. However, one skilled in the art could easily modify the exemplified studies to test the activity of polynucleotides or polypeptides of the invention (e.g., gene therapy).

Example 24 Biological Effects of Agonists or Antagonists of the Invention

Astrocyte and Neuronal Assays

Agonists or antagonists of the invention, expressed in Escherichia coli and purified as described above, can be tested for activity in promoting the survival, neurite outgrowth, or phenotypic differentiation of cortical neuronal cells and for inducing the proliferation of glial fibrillary acidic protein immunopositive cells, astrocytes. The selection of cortical cells for the bioassay is based on the prevalent expression of FGF-1 and FGF-2 in cortical structures and on the previously reported enhancement of cortical neuronal survival resulting from FGF-2 treatment. A thymidine incorporation assay, for example, can be used to elucidate an agonist or antagonist of the invention's activity on these cells.

Moreover, previous reports describing the biological effects of FGF-2 (basic FGF) on cortical or hippocampal neurons in vitro have demonstrated increases in both neuron survival and neurite outgrowth (Walicke et al., “Fibroblast growth factor promotes survival of dissociated hippocampal neurons and enhances neurite extension.” Proc. Natl. Acad. Sci. USA 83:3012-3016. (1986), assay herein incorporated by reference in its entirety). However, reports from experiments done on PC-12 cells suggest that these two responses are not necessarily synonymous and may depend on not only which FGF is being tested but also on which receptor(s) are expressed on the target cells. Using the primary cortical neuronal culture paradigm, the ability of an agonist or antagonist of the invention to induce neurite outgrowth can be compared to the response achieved with FGF-2 using, for example, a thymidine incorporation assay.

Fibroblast and Endothelial Cell Assays

Human lung fibroblasts are obtained from Clonetics (San Diego, Calif.) and maintained in growth media from Clonetics. Dermal microvascular endothelial cells are obtained from Cell Applications (San Diego, Calif.). For proliferation assays, the human lung fibroblasts and dermal microvascular endothelial cells can be cultured at 5,000 cells/well in a 96-well plate for one day in growth medium. The cells are then incubated for one day in 0.1% BSA basal medium. After replacing the medium with fresh 0.1% BSA medium, the cells are incubated with the test proteins for 3 days. ALAMAR BLUE™ (Alamar Biosciences, Sacramento, Calif.) is added to each well to a final concentration of 10%. The cells are incubated for 4 hr. Cell viability is measured by reading in a CYTOFLUOR™ fluorescence reader. For the PGE₂ assays, the human lung fibroblasts are cultured at 5,000 cells/well in a 96-well plate for one day. After a medium change to 0.1% BSA basal medium, the cells are incubated with FGF-2 or agonists or antagonists of the invention with or without IL-1α for 24 hours. The supernatants are collected and assayed for PGE₂ by EIA kit (Cayman, Ann Arbor, Mich.). For the IL-6 assays, the human lung fibroblasts are cultured at 5,000 cells/well in a 96-well plate for one day. After a medium change to 0.1% BSA basal medium, the cells are incubated with FGF-2 or with or without agonists or antagonists of the invention IL-1α for 24 hours. The supernatants are collected and assayed for IL-6 by ELISA kit (Endogen, Cambridge, Mass.).

Human lung fibroblasts are cultured with FGF-2 or agonists or antagonists of the invention for 3 days in basal medium before the addition of ALAMAR BLUE™ to assess effects on growth of the fibroblasts. FGF-2 should show a stimulation at 10-2500 ng/ml which can be used to compare stimulation with agonists or antagonists of the invention.

Parkinson Models.

The loss of motor function in Parkinson's disease is attributed to a deficiency of striatal dopamine resulting from the degeneration of the nigrostriatal dopaminergic projection neurons. An animal model for Parkinson's that has been extensively characterized involves the systemic administration of 1-methyl-4 phenyl 1,2,3,6-tetrahydropyridine (MPTP). In the CNS, MPTP is taken-up by astrocytes and catabolized by monoamine oxidase B to 1-methyl-4-phenyl pyridine (MPP⁺) and released. Subsequently, MPP⁺ is actively accumulated in dopaminergic neurons by the high-affinity reuptake transporter for dopamine. MPP⁺ is then concentrated in mitochondria by the electrochemical gradient and selectively inhibits nicotidamide adenine disphosphate: ubiquinone oxidoreductionase (complex I), thereby interfering with electron transport and eventually generating oxygen radicals.

It has been demonstrated in tissue culture paradigms that FGF-2 (basic FGF) has trophic activity towards nigral dopaminergic neurons (Ferrari et al., Dev. Biol. 1989). Recently, Dr. Unsicker's group has demonstrated that administering FGF-2 in gel foam implants in the striatum results in the near complete protection of nigral dopaminergic neurons from the toxicity associated with MPTP exposure (Otto and Unsicker, J. Neuroscience, 1990).

Based on the data with FGF-2, agonists or antagonists of the invention can be evaluated to determine whether it has an action similar to that of FGF-2 in enhancing dopaminergic neuronal survival in vitro and it can also be tested in vivo for protection of dopaminergic neurons in the striatum from the damage associated with MPTP treatment. The potential effect of an agonist or antagonist of the invention is first examined in vitro in a dopaminergic neuronal cell culture paradigm. The cultures are prepared by dissecting the midbrain floor plate from gestation day 14 Wistar rat embryos. The tissue is dissociated with trypsin and seeded at a density of 200,000 cells/cm² on polyorthinine-laminin coated glass coverslips. The cells are maintained in Dulbecco's Modified Eagle's medium and F12 medium containing hormonal supplements (N1). The cultures are fixed with paraformaldehyde after 8 days in vitro and are processed for tyrosine hydroxylase, a specific marker for dopaminergic neurons, immunohistochemical staining. Dissociated cell cultures are prepared from embryonic rats. The culture medium is changed every third day and the factors are also added at that time.

Since the dopaminergic neurons are isolated from animals at gestation day 14, a developmental time which is past the stage when the dopaminergic precursor cells are proliferating, an increase in the number of tyrosine hydroxylase immunopositive neurons would represent an increase in the number of dopaminergic neurons surviving in vitro. Therefore, if an agonist or antagonist of the invention acts to prolong the survival of dopaminergic neurons, it would suggest that the agonist or antagonist may be involved in Parkinson's Disease.

The studies described in this example tested activity of agonists or antagonists of the invention. However, one skilled in the art could easily modify the exemplified studies to test the activity of polynucleotides or polypeptides of the invention (e.g., gene therapy).

Example 25 The Effect of Agonists or Antagonists of the Invention on the Growth of Vascular Endothelial Cells

On day 1, human umbilical vein endothelial cells (HUVEC) are seeded at 2-5×10⁴ cells/35 mm dish density in M199 medium containing 4% fetal bovine serum (FBS), 16 units/ml heparin, and 50 units/ml endothelial cell growth supplements (ECGS, Biotechnique, Inc.). On day 2, the medium is replaced with M199 containing 10% FBS, 8 units/ml heparin. An agonist or antagonist of the invention, and positive controls, such as VEGF and basic FGF (bFGF) are added, at varying concentrations. On days 4 and 6, the medium is replaced. On day 8, cell number is determined with a Coulter Counter.

An increase in the number of HUVEC cells indicates that the compound of the invention may proliferate vascular endothelial cells, while a decrease in the number of HUVEC cells indicates that the compound of the invention inhibits vascular endothelial cells.

The studies described in this example tested activity of a polypeptide of the invention. However, one skilled in the art could easily modify the exemplified studies to test the activity of polynucleotides (e.g., gene therapy), agonists, and/or antagonists of the invention.

Example 26 Rat Corneal Wound Healing Model

This animal model shows the effect of an agonist or antagonist of the invention on neovascularization. The experimental protocol includes:

Making a 1-1.5 mm long incision from the center of cornea into the stromal layer.

Inserting a spatula below the lip of the incision facing the outer corner of the eye.

Making a pocket (its base is 1-1.5 mm form the edge of the eye).

Positioning a pellet, containing 50 ng-5 ug of an agonist or antagonist of the invention, within the pocket.

Treatment with an agonist or antagonist of the invention can also be applied topically to the corneal wounds in a dosage range of 20 mg-500 mg (daily treatment for five days).

The studies described in this example tested activity of agonists or antagonists of the invention. However, one skilled in the art could easily modify the exemplified studies to test the activity of polynucleotides or polypeptides of the invention (e.g., gene therapy).

Example 27 Diabetic Mouse and Glucocorticoid-Impaired Wound Healing Models

Diabetic db+/db+ Mouse Model

To demonstrate that an agonist or antagonist of the invention accelerates the healing process, the genetically diabetic mouse model of wound healing is used. The full thickness wound healing model in the db+/db+ mouse is a well characterized, clinically relevant and reproducible model of impaired wound healing. Healing of the diabetic wound is dependent on formation of granulation tissue and re-epithelialization rather than contraction (Gartner, M. H. et al., J. Surg. Res. 52:389 (1992); Greenhalgh, D. G. et al., Am. J. Pathol. 136:1235 (1990)).

The diabetic animals have many of the characteristic features observed in Type II diabetes mellitus. Homozygous (db+/db+) mice are obese in comparison to their normal heterozygous (db+/+m) littermates. Mutant diabetic (db+/db+) mice have a single autosomal recessive mutation on chromosome 4 (db+) (Coleman et al. Proc. Natl. Acad. Sci. USA 77:283-293 (1982)). Animals show polyphagia, polydipsia and polyuria. Mutant diabetic mice (db+/db+) have elevated blood glucose, increased or normal insulin levels, and suppressed cell-mediated immunity (Mandel et al., J. Immunol. 120:1375 (1978); Debray-Sachs, M. et al., Clin. Exp. Immunol 51(1):1-7 (1983); Leiter et al., Am. J. of Pathol 114:46-55 (1985)). Peripheral neuropathy, myocardial complications, and microvascular lesions, basement membrane thickening and glomerular filtration abnormalities have been described in these animals (Norido, F. et al., Exp. Neurol 83(2):221-232 (1984); Robertson et al., Diabetes 29(1):60-67 (1980); Giacomelli et al., Lab Invest. 40(4):460-473 (1979); Coleman, D. L., Diabetes 31 (Suppl):1-6 (1982)). These homozygous diabetic mice develop hyperglycemia that is resistant to insulin analogous to human type II diabetes (Mandel et al., J. Immunol. 120:1375-1377 (1978)).

The characteristics observed in these animals suggests that healing in this model may be similar to the healing observed in human diabetes (Greenhalgh, et al., Am. J. of Pathol. 136:1235-1246 (1990)).

Genetically diabetic female C57BL/KsJ (db+/db+) mice and their non-diabetic (db+/+m) heterozygous littermates are used in this study (Jackson Laboratories). The animals are purchased at 6 weeks of age and are 8 weeks old at the beginning of the study. Animals are individually housed and received food and water ad libitum. All manipulations are performed using aseptic techniques. The experiments are conducted according to the rules and guidelines of Human Genome Sciences, Inc. Institutional Animal Care and Use Committee and the Guidelines for the Care and Use of Laboratory Animals.

Wounding protocol is performed according to previously reported methods (Tsuboi, R. and Rifkin, D. B., J. Exp. Med. 172:245-251 (1990)). Briefly, on the day of wounding, animals are anesthetized with an intraperitoneal injection of Avertin (0.01 mg/mL), 2,2,2-tribromoethanol and 2-methyl-2-butanol dissolved in deionized water. The dorsal region of the animal is shaved and the skin washed with 70% ethanol solution and iodine. The surgical area is dried with sterile gauze prior to wounding. An 8 mm full-thickness wound is then created using a Keyes tissue punch. Immediately following wounding, the surrounding skin is gently stretched to eliminate wound expansion. The wounds are left open for the duration of the experiment. Application of the treatment is given topically for 5 consecutive days commencing on the day of wounding. Prior to treatment, wounds are gently cleansed with sterile saline and gauze sponges.

Wounds are visually examined and photographed at a fixed distance at the day of surgery and at two day intervals thereafter. Wound closure is determined by daily measurement on days 1-5 and on day 8. Wounds are measured horizontally and vertically using a calibrated Jameson caliper. Wounds are considered healed if granulation tissue is no longer visible and the wound is covered by a continuous epithelium.

An agonist or antagonist of the invention is administered using at a range different doses, from 4 mg to 500 mg per wound per day for 8 days in vehicle. Vehicle control groups received 50 mL of vehicle solution.

Animals are euthanized on day 8 with an intraperitoneal injection of sodium pentobarbital (300 mg/kg). The wounds and surrounding skin are then harvested for histology and immunohistochemistry. Tissue specimens are placed in 10% neutral buffered formalin in tissue cassettes between biopsy sponges for further processing.

Three groups of 10 animals each (5 diabetic and 5 non-diabetic controls) are evaluated: 1) Vehicle placebo control, 2) untreated group, and 3) treated group.

Wound closure is analyzed by measuring the area in the vertical and horizontal axis and obtaining the total square area of the wound. Contraction is then estimated by establishing the differences between the initial wound area (day 0) and that of post treatment (day 8). The wound area on day 1 is 64 mm², the corresponding size of the dermal punch. Calculations are made using the following formula: [Open area on day 8]−[Open area on day 1]/[Open area on day 1]

Specimens are fixed in 10% buffered formalin and paraffin embedded blocks are sectioned perpendicular to the wound surface (5 mm) and cut using a Reichert-Jung microtome. Routine hematoxylin-eosin (H&E) staining is performed on cross-sections of bisected wounds. Histologic examination of the wounds are used to assess whether the healing process and the morphologic appearance of the repaired skin is altered by treatment with an agonist or antagonist of the invention. This assessment included verification of the presence of cell accumulation, inflammatory cells, capillaries, fibroblasts, re-epithelialization and epidermal maturity (Greenhalgh, D. G. et al., Am. J. Pathol 136:1235 (1990)). A calibrated lens micrometer is used by a blinded observer.

Tissue sections are also stained immunohistochemically with a polyclonal rabbit anti-human keratin antibody using ABC Elite detection system. Human skin is used as a positive tissue control while non-immune IgG is used as a negative control. Keratinocyte growth is determined by evaluating the extent of reepithelialization of the wound using a calibrated lens micrometer.

Proliferating cell nuclear antigen/cyclin (PCNA) in skin specimens is demonstrated by using anti-PCNA antibody (1:50) with an ABC Elite detection system. Human colon cancer served as a positive tissue control and human brain tissue is used as a negative tissue control. Each specimen included a section with omission of the primary antibody and substitution with non-immune mouse IgG. Ranking of these sections is based on the extent of proliferation on a scale of 0-8, the lower side of the scale reflecting slight proliferation to the higher side reflecting intense proliferation.

Experimental data are analyzed using an unpaired t test. A p value of <0.05 is considered significant.

Steroid Impaired Rat Model

The inhibition of wound healing by steroids has been well documented in various in vitro and in vivo systems (Wahl, Glucocorticoids and Wound healing. In: Anti-Inflammatory Steroid Action: Basic and Clinical Aspects. 280-302 (1989); Wahl et al, J. Immunol. 115: 476-481 (1975); Werb et al., J. Exp. Med. 147:1684-1694 (1978)). Glucocorticoids retard wound healing by inhibiting angiogenesis, decreasing vascular permeability (Ebert et al., An. Intern. Med. 37:701-705 (1952)), fibroblast proliferation, and collagen synthesis (Beck et al., Growth Factors. 5: 295-304 (1991); Haynes et al., J. Clin. Invest. 61: 703-797 (1978)) and producing a transient reduction of circulating monocytes (Haynes et al., J. Clin. Invest. 61: 703-797 (1978); Wahl, “Glucocorticoids and wound healing”, In: Antiinflammatory Steroid Action: Basic and Clinical Aspects, Academic Press, New York, pp. 280-302 (1989)). The systemic administration of steroids to impaired wound healing is a well establish phenomenon in rats (Beck et al., Growth Factors. 5: 295-304 (1991); Haynes et al., J. Clin. Invest. 61: 703-797 (1978); Wahl, “Glucocorticoids and wound healing”, In: Antiinflammatory Steroid Action: Basic and Clinical Aspects, Academic Press, New York, pp. 280-302 (1989); Pierce et al., Proc. Natl. Acad. Sci. USA 86: 2229-2233 (1989)).

To demonstrate that an agonist or antagonist of the invention can accelerate the healing process, the effects of multiple topical applications of the agonist or antagonist on full thickness excisional skin wounds in rats in which healing has been impaired by the systemic administration of methylprednisolone is assessed.

Young adult male Sprague Dawley rats weighing 250-300 g (Charles River Laboratories) are used in this example. The animals are purchased at 8 weeks of age and are 9 weeks old at the beginning of the study. The healing response of rats is impaired by the systemic administration of methylprednisolone (17 mg/kg/rat intramuscularly) at the time of wounding. Animals are individually housed and received food and water ad libitum. All manipulations are performed using aseptic techniques. This study is conducted according to the rules and guidelines of Human Genome Sciences, Inc. Institutional Animal Care and Use Committee and the Guidelines for the Care and Use of Laboratory Animals.

The wounding protocol is followed according to section A, above. On the day of wounding, animals are anesthetized with an intramuscular injection of ketamine (50 mg/kg) and xylazine (5 mg/kg). The dorsal region of the animal is shaved and the skin washed with 70% ethanol and iodine solutions. The surgical area is dried with sterile gauze prior to wounding. An 8 mm full-thickness wound is created using a Keyes tissue punch. The wounds are left open for the duration of the experiment. Applications of the testing materials are given topically once a day for 7 consecutive days commencing on the day of wounding and subsequent to methylprednisolone administration. Prior to treatment, wounds are gently cleansed with sterile saline and gauze sponges.

Wounds are visually examined and photographed at a fixed distance at the day of wounding and at the end of treatment. Wound closure is determined by daily measurement on days 1-5 and on day 8. Wounds are measured horizontally and vertically using a calibrated Jameson caliper. Wounds are considered healed if granulation tissue is no longer visible and the wound is covered by a continuous epithelium.

The agonist or antagonist of the invention is administered using at a range different doses, from 4 mg to 500 mg per wound per day for 8 days in vehicle. Vehicle control groups received 50 mL of vehicle solution.

Animals are euthanized on day 8 with an intraperitoneal injection of sodium pentobarbital (300 mg/kg). The wounds and surrounding skin are then harvested for histology. Tissue specimens are placed in 10% neutral buffered formalin in tissue cassettes between biopsy sponges for further processing.

Three groups of 10 animals each (5 with methylprednisolone and 5 without glucocorticoid) are evaluated: 1) Untreated group 2) Vehicle placebo control 3) treated groups.

Wound closure is analyzed by measuring the area in the vertical and horizontal axis and obtaining the total area of the wound. Closure is then estimated by establishing the differences between the initial wound area (day 0) and that of post treatment (day 8). The wound area on day 1 is 64 mm², the corresponding size of the dermal punch. Calculations are made using the following formula: [Open area on day 8]−[Open area on day 1]/[Open area on day 1]

Specimens are fixed in 10% buffered formalin and paraffin embedded blocks are sectioned perpendicular to the wound surface (5 mm) and cut using an Olympus microtome. Routine hematoxylin-eosin (H&E) staining is performed on cross-sections of bisected wounds. Histologic examination of the wounds allows assessment of whether the healing process and the morphologic appearance of the repaired skin is improved by treatment with an agonist or antagonist of the invention. A calibrated lens micrometer is used by a blinded observer to determine the distance of the wound gap.

Experimental data are analyzed using an unpaired t test. A p value of <0.05 is considered significant.

The studies described in this example tested activity of agonists or antagonists of the invention. However, one skilled in the art could easily modify the exemplified studies to test the activity of polynucleotides or polypeptides of the invention (e.g., gene therapy).

Example 28 Lymphadema Animal Model

The purpose of this experimental approach is to create an appropriate and consistent lymphedema model for testing the therapeutic effects of an agonist or antagonist of the invention in lymphangiogenesis and re-establishment of the lymphatic circulatory system in the rat hind limb. Effectiveness is measured by swelling volume of the affected limb, quantification of the amount of lymphatic vasculature, total blood plasma protein, and histopathology. Acute lymphedema is observed for 7-10 days. Perhaps more importantly, the chronic progress of the edema is followed for up to 3-4 weeks.

Prior to beginning surgery, blood sample is drawn for protein concentration analysis. Male rats weighing approximately ˜350 g are dosed with Pentobarbital. Subsequently, the right legs are shaved from knee to hip. The shaved area is swabbed with gauze soaked in 70% EtOH. Blood is drawn for serum total protein testing. Circumference and volumetric measurements are made prior to injecting dye into paws after marking 2 measurement levels (0.5 cm above heel, at mid-pt of dorsal paw). The intradermal dorsum of both right and left paws are injected with 0.05 ml of 1% Evan's Blue. Circumference and volumetric measurements are then made following injection of dye into paws.

Using the knee joint as a landmark, a mid-leg inguinal incision is made circumferentially allowing the femoral vessels to be located. Forceps and hemostats are used to dissect and separate the skin flaps. After locating the femoral vessels, the lymphatic vessel that runs along side and underneath the vessel(s) is located. The main lymphatic vessels in this area are then electrically coagulated or suture ligated.

Using a microscope, muscles in back of the leg (near the semitendinosis and adductors) are bluntly dissected. The popliteal lymph node is then located. The 2 proximal and 2 distal lymphatic vessels and distal blood supply of the popliteal node are then ligated by suturing. The popliteal lymph node, and any accompanying adipose tissue, is then removed by cutting connective tissues.

Care is taken to control any mild bleeding resulting from this procedure. After lymphatics are occluded, the skin flaps are sealed by using liquid skin (Vetbond) (AJ Buck). The separated skin edges are sealed to the underlying muscle tissue while leaving a gap of ˜0.5 cm around the leg. Skin also may be anchored by suturing to underlying muscle when necessary.

To avoid infection, animals are housed individually with mesh (no bedding). Recovering animals are checked daily through the optimal edematous peak, which typically occurred by day 5-7. The plateau edematous peak are then observed. To evaluate the intensity of the lymphedema, the circumference and volumes of 2 designated places on each paw before operation and daily for 7 days are measured. The effect of plasma proteins on lymphedema is determined and whether protein analysis is a useful testing perimeter is also investigated. The weights of both control and edematous limbs are evaluated at 2 places. Analysis is performed in a blind manner.

Circumference Measurements: Under brief gas anesthetic to prevent limb movement, a cloth tape is used to measure limb circumference. Measurements are done at the ankle bone and dorsal paw by 2 different people and those 2 readings are averaged. Readings are taken from both control and edematous limbs.

Volumetric Measurements: On the day of surgery, animals are anesthetized with Pentobarbital and are tested prior to surgery. For daily volumetrics animals are under brief halothane anesthetic (rapid immobilization and quick recovery), and both legs are shaved and equally marked using waterproof marker on legs. Legs are first dipped in water, then dipped into instrument to each marked level then measured by Buxco edema software(Chen/Victor). Data is recorded by one person, while the other is dipping the limb to marked area.

Blood-plasma protein measurements: Blood is drawn, spun, and serum separated prior to surgery and then at conclusion for total protein and Ca²⁺ comparison.

Limb Weight Comparison: After drawing blood, the animal is prepared for tissue collection. The limbs are amputated using a quillitine, then both experimental and control legs are cut at the ligature and weighed. A second weighing is done as the tibio-cacaneal joint is disarticulated and the foot is weighed.

Histological Preparations: The transverse muscle located behind the knee (popliteal) area is dissected and arranged in a metal mold, filled with freezeGel, dipped into cold methylbutane, placed into labeled sample bags at −80EC until sectioning. Upon sectioning, the muscle is observed under fluorescent microscopy for lymphatics.

The studies described in this example tested activity of agonists or antagonists of the invention. However, one skilled in the art could easily modify the exemplified studies to test the activity of polynucleotides or polypeptides of the invention (e.g., gene therapy).

Example 29 Suppression of TNF Alpha-Induced Adhesion Molecule Expression by an Agonist or Antagonist of the Invention

The recruitment of lymphocytes to areas of inflammation and angiogenesis involves specific receptor-ligand interactions between cell surface adhesion molecules (CAMs) on lymphocytes and the vascular endothelium. The adhesion process, in both normal and pathological settings, follows a multi-step cascade that involves intercellular adhesion molecule-1 (ICAM-1), vascular cell adhesion molecule-1 (VCAM-1), and endothelial leukocyte adhesion molecule-1 (E-selectin) expression on endothelial cells (EC). The expression of these molecules and others on the vascular endothelium determines the efficiency with which leukocytes may adhere to the local vasculature and extravasate into the local tissue during the development of an inflammatory response. The local concentration of cytokines and growth factor participate in the modulation of the expression of these CAMs.

Tumor necrosis factor alpha (TNF-a), a potent proinflammatory cytokine, is a stimulator of all three CAMs on endothelial cells and may be involved in a wide variety of inflammatory responses, often resulting in a pathological outcome.

The potential of an agonist or antagonist of the invention to mediate a suppression of TNF-a induced CAM expression can be examined. A modified ELISA assay which uses ECs as a solid phase absorbent is employed to measure the amount of CAM expression on TNF-a treated ECs when co-stimulated with a member of the FGF family of proteins.

To perform the experiment, human umbilical vein endothelial cell (HUVEC) cultures are obtained from pooled cord harvests and maintained in growth medium (EGM-2; Clonetics, San Diego, Calif.) supplemented with 10% FCS and 1% penicillin/streptomycin in a 37 degree C. humidified incubator containing 5% CO₂. HUVECs are seeded in 96-well plates at concentrations of 1×10⁴ cells/well in EGM medium at 37 degree C. for 18-24 hrs or until confluent. The monolayers are subsequently washed 3 times with a serum-free solution of RPMI-1640 supplemented with 100 U/ml penicillin and 100 mg/ml streptomycin, and treated with a given cytokine and/or growth factor(s) for 24 h at 37 degree C. Following incubation, the cells are then evaluated for CAM expression.

Human Umbilical Vein Endothelial cells (HUVECs) are grown in a standard 96 well plate to confluence. Growth medium is removed from the cells and replaced with 90 ul of 199 Medium (10% FBS). Samples for testing and positive or negative controls are added to the plate in triplicate (in 10 ul volumes). Plates are incubated at 37 degree C. for either 5 h (selectin and integrin expression) or 24 h (integrin expression only). Plates are aspirated to remove medium and 100 μl of 0.1% paraformaldehyde-PBS(with Ca++ and Mg++) is added to each well. Plates are held at 4° C. for 30 min.

Fixative is then removed from the wells and wells are washed 1× with PBS(+Ca,Mg)+0.5% BSA and drained. Do not allow the wells to dry. Add 10 μl of diluted primary antibody to the test and control wells. Anti-ICAM-1-Biotin, Anti-VCAM-1-Biotin and Anti-E-selectin-Biotin are used at a concentration of 10 μg/ml (1:10 dilution of 0.1 mg/ml stock antibody). Cells are incubated at 37° C. for 30 min. in a humidified environment. Wells are washed ×3 with PBS(+Ca,Mg)+0.5% BSA.

Then add 20 μl of diluted EXTRAVIDIN™-Alkaline Phosphotase (1:5,000 dilution) to each well and incubated at 37° C. for 30 min. Wells are washed ×3 with PBS(+Ca,Mg)+0.5% BSA. 1 tablet of p-Nitrophenol Phosphate pNPP is dissolved in 5 ml of glycine buffer (pH 10.4). 100 μl of pNPP substrate in glycine buffer is added to each test well. Standard wells in triplicate are prepared from the working dilution of the EXTRAVIDIN™-Alkaline Phosphotase in glycine buffer: 1:5,000 (10⁰)>10^(−0.5)>10⁻¹>10^(−1.5) 0.5 μl of each dilution is added to triplicate wells and the resulting AP content in each well is 5.50 ng, 1.74 ng, 0.55 ng, 0.18 ng. 100 μl of pNNP reagent must then be added to each of the standard wells. The plate must be incubated at 37° C. for 4 h. A volume of 50 μl of 3M NaOH is added to all wells. The results are quantified on a plate reader at 405 nm. The background subtraction option is used on blank wells filled with glycine buffer only. The template is set up to indicate the concentration of AP-conjugate in each standard well [5.50 ng; 1.74 ng; 0.55 ng; 0.18 ng]. Results are indicated as amount of bound AP-conjugate in each sample.

The studies described in this example tested activity of agonists or antagonists of the invention. However, one skilled in the art could easily modify the exemplified studies to test the activity of polynucleotides or polypeptides of the invention (e.g., gene therapy).

Example 30 Production of Polypeptide of the Invention for High-Throughput Screening Assays

The following protocol produces a supernatant containing polypeptide of the present invention to be tested. This supernatant can then be used in the Screening Assays described in Examples 32-41.

First, dilute Poly-D-Lysine (644 587 BOEHRINGER™-Mannheim) stock solution (1 mg/ml in PBS) 1:20 in PBS (w/o calcium or magnesium 17-516F Biowhittaker) for a working solution of 50 ug/ml. Add 200 ul of this solution to each well (24 well plates) and incubate at RT for 20 minutes. Be sure to distribute the solution over each well (note: a 12-channel pipetter may be used with tips on every other channel). Aspirate off the Poly-D-Lysine solution and rinse with 1 ml PBS (Phosphate Buffered Saline). The PBS should remain in the well until just prior to plating the cells and plates may be poly-lysine coated in advance for up to two weeks.

Plate 293T cells (do not carry cells past P+20) at 2×10⁵ cells/well in 0.5 ml DMEM(Dulbecco's Modified Eagle Medium)(with 4.5 G/L glucose and L-glutamine (12-604F Biowhittaker))/10% heat inactivated FBS(14-503F Biowhittaker)/1×Penstrep(17-602E Biowhittaker). Let the cells grow overnight.

The next day, mix together in a sterile solution basin: 300 ul Lipofectamine (18324-012 Gibco/BRL) and 5 ml Optimem 1 (31985070 Gibco/BRL)/96-well plate. With a small volume multi-channel pipetter, aliquot approximately 2 ug of an expression vector containing a polynucleotide insert, produced by the methods described in Examples 8-10, into an appropriately labeled 96-well round bottom plate. With a multi-channel pipetter, add 50 ul of the Lipofectamine/Optimem I mixture to each well. Pipette up and down gently to mix. Incubate at RT 15-45 minutes. After about 20 minutes, use a multi-channel pipetter to add 150 ul Optimem I to each well. As a control, one plate of vector DNA lacking an insert should be transfected with each set of transfections.

Preferably, the transfection should be performed by tag-teaming the following tasks. By tag-teaming, hands on time is cut in half, and the cells do not spend too much time on PBS. First, person A aspirates off the media from four 24-well plates of cells, and then person B rinses each well with 0.5-1 ml PBS. Person A then aspirates off PBS rinse, and person B, using a12-channel pipetter with tips on every other channel, adds the 200 ul of DNA/Lipofectamine/Optimem I complex to the odd wells first, then to the even wells, to each row on the 24-well plates. Incubate at 37 degree C. for 6 hours.

While cells are incubating, prepare appropriate media, either 1% BSA in DMEM with 1× penstrep, or HGS CHO-5 media (116.6 mg/L of CaCl₂ (anhyd); 0.00130 mg/L CuSO₄-5H₂O; 0.050 mg/L of Fe(NO₃)₃-9H₂O; 0.417 mg/L of FeSO₄-7H₂O; 311.80 mg/L of Kcl; 28.64 mg/L of MgCl₂; 48.84 mg/L of MgSO₄; 6995.50 mg/L of NaCl; 2400.0 mg/L of NaHCO₃; 62.50 mg/L of NaH₂PO₄—H₂0; 71.02 mg/L of Na₂HPO4; 0.4320 mg/L of ZnSO₄.7H₂O; 0.002 mg/L of Arachidonic Acid; 1.022 mg/L of Cholesterol; 0.070 mg/L of DL-alpha-Tocopherol-Acetate; 0.0520 mg/L of Linoleic Acid; 0.010 mg/L of Linolenic Acid; 0.010 mg/L of Myristic Acid; 0.010 mg/L of Oleic Acid; 0.010 mg/L of Palmitric Acid; 0.010 mg/L of Palmitic Acid; 100 mg/L of Pluronic F-68; 0.010 mg/L of Stearic Acid; 2.20 mg/L of Tween 80; 4551 mg/L of D-Glucose; 130.85 mg/ml of L-Alanine; 147.50 mg/ml of L-Arginine-HCL; 7.50 mg/ml of L-Asparagine-H₂O; 6.65 mg/ml of L-Aspartic Acid; 29.56 mg/ml of L-Cystine-2HCL-H₂O; 31.29 mg/ml of L-Cystine-2HCL; 7.35 mg/ml of L-Glutamic Acid; 365.0 mg/ml of L-Glutamine; 18.75 mg/ml of Glycine; 52.48 mg/ml of L-Histidine-HCL-H₂0; 106.97 mg/ml of L-Isoleucine; 111.45 mg/ml of L-Leucine; 163.75 mg/ml of L-Lysine HCL; 32.34 mg/ml of L-Methionine; 68.48 mg/ml of L-Phenylalainine; 40.0 mg/ml of L-Proline; 26.25 mg/ml of L-Serine; 101.05 mg/ml of L-Threonine; 19.22 mg/ml of L-Tryptophan; 91.79 mg/ml of L-Tryrosine-2Na-2H₂0; and 99.65 mg/ml of L-Valine; 0.0035 mg/L of Biotin; 3.24 mg/L of D-Ca Pantothenate; 11.78 mg/L of Choline Chloride; 4.65 mg/L of Folic Acid; 15.60 mg/L of i-Inositol; 3.02 mg/L of Niacinamide; 3.00 mg/L of Pyridoxal HCL; 0.031 mg/L of Pyridoxine HCL; 0.319 mg/L of Riboflavin; 3.17 mg/L of Thiamine HCL; 0.365 mg/L of Thymidine; 0.680 mg/L of Vitamin B₁₂; 25 mM of HEPES Buffer; 2.39 mg/L of Na Hypoxanthine; 0.105 mg/L of Lipoic Acid; 0.081 mg/L of Sodium Putrescine-2HCL; 55.0 mg/L of Sodium Pyruvate; 0.0067 mg/L of Sodium Selenite; 20 uM of Ethanolamine; 0.122 mg/L of Ferric Citrate; 41.70 mg/L of Methyl-B-Cyclodextrin complexed with Linoleic Acid; 33.33 mg/L of Methyl-B-Cyclodextrin complexed with Oleic Acid; 10 mg/L of Methyl-B-Cyclodextrin complexed with Retinal Acetate. Adjust osmolarity to 327 mOsm) with 2 mm glutamine and 1× penstrep. (BSA (81-068-3 BAYER™) 100 gm dissolved in 1 L DMEM for a 10% BSA stock solution). Filter the media and collect 50 ul for endotoxin assay in 15 ml polystyrene conical.

The transfection reaction is terminated, preferably by tag-teaming, at the end of the incubation period. Person A aspirates off the transfection media, while person B adds 1.5 ml appropriate media to each well. Incubate at 37 degree C. for 45 or 72 hours depending on the media used: 1% BSA for 45 hours or CHO-5 for 72 hours.

On day four, using a 300 ul multichannel pipetter, aliquot 600 ul in one 1 ml deep well plate and the remaining supernatant into a 2 ml deep well. The supernatants from each well can then be used in the assays described in Examples 32-39.

It is specifically understood that when activity is obtained in any of the assays described below using a supernatant, the activity originates from either the polypeptide of the present invention directly (e.g., as a secreted protein) or by polypeptide of the present invention inducing expression of other proteins, which are then secreted into the supernatant. Thus, the invention further provides a method of identifying the protein in the supernatant characterized by an activity in a particular assay.

Example 31 Construction of GAS Reporter Construct

One signal transduction pathway involved in the differentiation and proliferation of cells is called the Jaks-STATs pathway. Activated proteins in the Jaks-STATs pathway bind to gamma activation site “GAS” elements or interferon-sensitive responsive element (“ISRE”), located in the promoter of many genes. The binding of a protein to these elements alter the expression of the associated gene.

GAS and ISRE elements are recognized by a class of transcription factors called Signal Transducers and Activators of Transcription, or “STATs.” There are six members of the STATs family. Stat1 and Stat3 are present in many cell types, as is Stat2 (as response to IFN-alpha is widespread). Stat4 is more restricted and is not in many cell types though it has been found in T helper class I, cells after treatment with IL-12. Stat5 was originally called mammary growth factor, but has been found at higher concentrations in other cells including myeloid cells. It can be activated in tissue culture cells by many cytokines.

The STATs are activated to translocate from the cytoplasm to the nucleus upon tyrosine phosphorylation by a set of kinases known as the Janus Kinase (“Jaks”) family. Jaks represent a distinct family of soluble tyrosine kinases and include Tyk2, Jak1, Jak2, and Jak3. These kinases display significant sequence similarity and are generally catalytically inactive in resting cells.

The Jaks are activated by a wide range of receptors summarized in the Table below. (Adapted from review by Schidler and Damell, Ann. Rev. Biochem. 64:621-51 (1995)). A cytokine receptor family, capable of activating Jaks, is divided into two groups: (a) Class 1 includes receptors for IL-2, IL-3, IL-4, IL-6, IL-7, IL-9, IL-11, IL-12, IL-15, Epo, PRL, GH, G-CSF, GM-CSF, LIF, CNTF, and thrombopoietin; and (b) Class 2 includes IFN-α, IFN-g, and IL-10. The Class 1 receptors share a conserved cysteine motif (a set of four conserved cysteines and one tryptophan) and a WSXWS motif (a membrane proximal region encoding Trp-Ser-Xaa-Trp-Ser (SEQ ID NO: 2)).

Thus, on binding of a ligand to a receptor, Jaks are activated, which in turn activate STATs, which then translocate and bind to GAS elements. This entire process is encompassed in the Jaks-STATs signal transduction pathway. Therefore, activation of the Jaks-STATs pathway, reflected by the binding of the GAS or the ISRE element, can be used to indicate proteins involved in the proliferation and differentiation of cells. For example, growth factors and cytokines are known to activate the Jaks-STATs pathway (See Table below). Thus, by using GAS elements linked to reporter molecules, activators of the Jaks-STATs pathway can be identified. JAKs Ligand tyk2 Jak1 Jak2 Jak3 STATS GAS (elements) or ISRE IFN family IFN-a/B + + − − 1, 2, 3 ISRE IFN-g + + − 1 GAS (IRF1 > Lys6 > IFP) Il-10 + ? ? − 1, 3 gp130 family IL-6 (Pleiotropic) + + + ? 1, 3 GAS (IRF1 > Lys6 > IFP) Il-11 (Pleiotropic) ? + ? ? 1, 3 OnM (Pleiotropic) ? + + ? 1, 3 LIF (Pleiotropic) ? + + ? 1, 3 CNTF (Pleiotropic) −/+ + + ? 1, 3 G-CSF (Pleiotropic) ? + ? ? 1, 3 IL-12 (Pleiotropic) + − + + 1, 3 g-C family IL-2 (lymphocytes) − + − + 1, 3, 5 GAS IL-4 (lymph/myeloid) − + − + 6 GAS (IRF1 = IFP >> Ly6)(IgH) IL-7 (lymphocytes) − + − + 5 GAS IL-9 (lymphocytes) − + − + 5 GAS IL-13 (lymphocyte) − + ? ? 6 GAS IL-15 ? + ? + 5 GAS gp140 family IL-3 (myeloid) − − + − 5 GAS (IRF1 > IFP >> Ly6) IL-5 (myeloid) − − + − 5 GAS GM-CSF (myeloid) − − + − 5 GAS Growth hormone family GH ? − + − 5 PRL ? +/− + − 1, 3, 5 EPO ? − + − 5 GAS (B-CAS > IRF1 = IFP >> Ly6) Receptor Tyrosine Kinases EGF ? + + − 1, 3 GAS (IRF1) PDGF ? + + − 1, 3 CSF-1 ? + + − 1, 3 GAS (not IRF1)

To construct a synthetic GAS containing promoter element, which is used in the Biological Assays described in Examples 32-33, a PCR based strategy is employed to generate a GAS-SV40 promoter sequence. The 5′ primer contains four tandem copies of the GAS binding site found in the IRF 1 promoter and previously demonstrated to bind STATs upon induction with a range of cytokines (Rothman et al., Immunity 1:457-468 (1994).), although other GAS or ISRE elements can be used instead. The 5′ primer also contains 18 bp of sequence complementary to the SV40 early promoter sequence and is flanked with an XhoI site. The sequence of the 5′ primer is: (SEQ ID NO:3) 5′:GCGCCTCGAGATTTCCCCGAAATCTAGATTTCCCCGAAATGATTTCC CCGAAATGATTTCCCCGAAATATCTGCCATCTCAATTAG:3′

The downstream primer is complementary to the SV40 promoter and is flanked with a Hind III site: (SEQ ID NO:4) 5′:GCGGCAAGCTTTTTGCAAAGCCTAGGC:3′

PCR amplification is performed using the SV40 promoter template present in the B-gal:promoter plasmid obtained from CLONTECH™. The resulting PCR fragment is digested with XhoI/Hind III and subcloned into BLSK2-. (STRATAGENE™.) Sequencing with forward and reverse primers confirms that the insert contains the following sequence: (SEQ ID NO:5) 5′:CTCGAGATTTCCCCGAAATCTAGATTTCCCCGAAATGATTTCCCCGA AATGATTTCCCCGAAATATCTGCCATCTCAATTAGTCAGCAACCATAGTC CCGCCCCTAACTCCGCCCATCCCGCCCCTAACTCCGCCCAGTTCCGCCCA TTCTCCGCCCCATGGCTGACTAATTTTTTTTATTTATGCAGAGGCCGAGG CCGCCTCGGCCTCTGAGCTATTCCAGAAGTAGTGAGGAGGCTTTTTTGGA GGCCTAGGCTTTTGCAAAAAGCTT:3′

With this GAS promoter element linked to the SV40 promoter, a GAS: SEAP2 reporter construct is next engineered. Here, the reporter molecule is a secreted alkaline phosphatase, or “SEAP.” Clearly, however, any reporter molecule can be instead of SEAP, in this or in any of the other Examples. Well known reporter molecules that can be used instead of SEAP include chloramphenicol acetyltransferase (CAT), luciferase, alkaline phosphatase, B-galactosidase, green fluorescent protein (GFP), or any protein detectable by an antibody.

The above sequence confirmed synthetic GAS-SV40 promoter element is subcloned into the pSEAP-Promoter vector obtained from CLONTECH™ using HindIII and XhoI, effectively replacing the SV40 promoter with the amplified GAS:SV40 promoter element, to create the GAS-SEAP vector. However, this vector does not contain a neomycin resistance gene, and therefore, is not preferred for mammalian expression systems.

Thus, in order to generate mammalian stable cell lines expressing the GAS-SEAP reporter, the GAS-SEAP cassette is removed from the GAS-SEAP vector using SalI and NotI, and inserted into a backbone vector containing the neomycin resistance gene, such as pGFP-1 (CLONTECH™), using these restriction sites in the multiple cloning site, to create the GAS-SEAP/Neo vector. Once this vector is transfected into mammalian cells, this vector can then be used as a reporter molecule for GAS binding as described in Examples 32-33.

Other constructs can be made using the above description and replacing GAS with a different promoter sequence. For example, construction of reporter molecules containing EGR and NF-KB promoter sequences are described in Examples 34 and 35. However, many other promoters can be substituted using the protocols described in these Examples. For instance, SRE, IL-2, NFAT, or Osteocalcin promoters can be substituted, alone or in combination (e.g., GAS/NF-KB/EGR, GAS/NF-KB, II-2/NFAT, or NF-KB/GAS). Similarly, other cell lines can be used to test reporter construct activity, such as HELA (epithelial), HUVEC (endothelial), Reh (B-cell), Saos-2 (osteoblast), HUVAC (aortic), or Cardiomyocyte.

Example 32 High-Throughput Screening Assay for T-cell Activity

The following protocol is used to assess T-cell activity by identifying factors, and determining whether supernate containing a polypeptide of the invention proliferates and/or differentiates T-cells. T-cell activity is assessed using the GAS/SEAP/Neo construct produced in Example 31. Thus, factors that increase SEAP activity indicate the ability to activate the Jaks-STATS signal transduction pathway. The T-cell used in this assay is Jurkat T-cells (ATCC™ Accession No. TIB-152), although Molt-3 cells (ATCC™ Accession No. CRL-1552) and Molt-4 cells (ATCC™ Accession No. CRL-1582) cells can also be used.

Jurkat T-cells are lymphoblastic CD4+ Th1 helper cells. In order to generate stable cell lines, approximately 2 million Jurkat cells are transfected with the GAS-SEAP/neo vector using DMRIE-C (LIFE TECHNOLOGIES™)(transfection procedure described below). The transfected cells are seeded to a density of approximately 20,000 cells per well and transfectants resistant to 1 mg/ml genticin selected. Resistant colonies are expanded and then tested for their response to increasing concentrations of interferon gamma. The dose response of a selected clone is demonstrated.

Specifically, the following protocol will yield sufficient cells for 75 wells containing 200 ul of cells. Thus, it is either scaled up, or performed in multiple to generate sufficient cells for multiple 96 well plates. Jurkat cells are maintained in RPMI+10% serum with 1% Pen-Strep. Combine 2.5 mls of OPTI-MEM™ (LIFE TECHNOLOGIES™) with 10 ug of plasmid DNA in a T25 flask. Add 2.5 ml OPTI-MEM™ containing 50 ul of DMRIE-C and incubate at room temperature for 15-45 mins.

During the incubation period, count cell concentration, spin down the required number of cells (107 per transfection), and resuspend in OPTI-MEM™ to a final concentration of 10⁷ cells/ml. Then add 1 ml of 1×10⁷ cells in OPTI-MEM™ to T25 flask and incubate at 37 degree C. for 6 hrs. After the incubation, add 10 ml of RPMI+15% serum.

The Jurkat:GAS-SEAP stable reporter lines are maintained in RPMI+10% serum, 1 mg/ml Genticin, and 1% Pen-Strep. These cells are treated with supernatants containing polypeptide of the present invention or polypeptide of the present invention induced polypeptides as produced by the protocol described in Example 30.

On the day of treatment with the supernatant, the cells should be washed and resuspended in fresh RPMI+10% serum to a density of 500,000 cells per ml. The exact number of cells required will depend on the number of supernatants being screened. For one 96 well plate, approximately 10 million cells (for 10 plates, 100 million cells) are required.

Transfer the cells to a triangular reservoir boat, in order to dispense the cells into a 96 well dish, using a 12 channel pipette. Using a 12 channel pipette, transfer 200 ul of cells into each well (therefore adding 100,000 cells per well).

After all the plates have been seeded, 50 ul of the supernatants are transferred directly from the 96 well plate containing the supernatants into each well using a 12 channel pipette. In addition, a dose of exogenous interferon gamma (0.1, 1.0, 10 ng) is added to wells H9, H10, and H11 to serve as additional positive controls for the assay.

The 96 well dishes containing Jurkat cells treated with supernatants are placed in an incubator for 48 hrs (note: this time is variable between 48-72 hrs). 35 ul samples from each well are then transferred to an opaque 96 well plate using a 12 channel pipette. The opaque plates should be covered (using sellophene covers) and stored at −20 degree C. until SEAP assays are performed according to Example 36. The plates containing the remaining treated cells are placed at 4 degree C. and serve as a source of material for repeating the assay on a specific well if desired.

As a positive control, 100 Unit/ml interferon gamma can be used which is known to activate Jurkat T cells. Over 30 fold induction is typically observed in the positive control wells.

The above protocol may be used in the generation of both transient, as well as, stable transfected cells, which would be apparent to those of skill in the art.

Example 33 High-Throughput Screening Assay Identifying Myeloid Activity

The following protocol is used to assess myeloid activity of polypeptide of the present invention by determining whether polypeptide of the present invention proliferates and/or differentiates myeloid cells. Myeloid cell activity is assessed using the GAS/SEAP/Neo construct produced in Example 31. Thus, factors that increase SEAP activity indicate the ability to activate the Jaks-STATS signal transduction pathway. The myeloid cell used in this assay is U937, a pre-monocyte cell line, although TF-1, HL60, or KG1 can be used.

To transiently transfect U937 cells with the GAS/SEAP/Neo construct produced in Example 31, a DEAE-Dextran method (Kharbanda et. al., 1994, Cell Growth & Differentiation, 5:259-265) is used. First, harvest 2×10⁷ U937 cells and wash with PBS. The U937 cells are usually grown in RPMI 1640 medium containing 10% heat-inactivated fetal bovine serum (FBS) supplemented with 100 units/ml penicillin and 100 mg/ml streptomycin.

Next, suspend the cells in 1 ml of 20 mM Tris-HCl (pH 7.4) buffer containing 0.5 mg/ml DEAE-Dextran, 8 ug GAS-SEAP2 plasmid DNA, 140 mM NaCl, 5 mM KCl, 375 uM Na₂HPO₄.7H₂O, 1 mM MgCl₂, and 675 uM CaCl₂. Incubate at 37 degrees C. for 45 min.

Wash the cells with RPMI 1640 medium containing 10% FBS and then resuspend in 10 ml complete medium and incubate at 37 degree C. for 36 hr.

The GAS-SEAP/U937 stable cells are obtained by growing the cells in 400 ug/ml G418. The G418-free medium is used for routine growth but every one to two months, the cells should be re-grown in 400 ug/ml G418 for couple of passages.

These cells are tested by harvesting 1×10⁸ cells (this is enough for ten 96-well plates assay) and wash with PBS. Suspend the cells in 200 ml above described growth medium, with a final density of 5×10⁵ cells/ml. Plate 200 ul cells per well in the 96-well plate (or 1×10⁵ cells/well).

Add 50 ul of the supernatant prepared by the protocol described in Example 30. Incubate at 37 degee C for 48 to 72 hr. As a positive control, 100 Unit/ml interferon gamma can be used which is known to activate U937 cells. Over 30 fold induction is typically observed in the positive control wells. SEAP assay the supernatant according to the protocol described in Example 36.

Example 34 High-Throughput Screening Assay Identifying Neuronal Activity

When cells undergo differentiation and proliferation, a group of genes are activated through many different signal transduction pathways. One of these genes, EGR1 (early growth response gene 1), is induced in various tissues and cell types upon activation. The promoter of EGR1 is responsible for such induction. Using the EGR1 promoter linked to reporter molecules, activation of cells can be assessed by polypeptide of the present invention.

Particularly, the following protocol is used to assess neuronal activity in PC12 cell lines. PC12 cells (rat phenochromocytoma cells) are known to proliferate and/or differentiate by activation with a number of mitogens, such as TPA (tetradecanoyl phorbol acetate), NGF (nerve growth factor), and EGF (epidermal growth factor). The EGR1 gene expression is activated during this treatment. Thus, by stably transfecting PC 12 cells with a construct containing an EGR promoter linked to SEAP reporter, activation of PC 12 cells by polypeptide of the present invention can be assessed.

The EGR/SEAP reporter construct can be assembled by the following protocol. The EGR-1 promoter sequence (−633 to +1)(Sakamoto K et al., Oncogene 6:867-871 (1991)) can be PCR amplified from human genomic DNA using the following primers: (SEQ ID NO:6) 5′ GCGCTCGAGGGATGACAGCGATAGAACCCCGG-3′ (SEQ ID NO:7) 5′ GCGAAGCTTCGCGACTCCCCGGATCCGCCTC-3′

Using the GAS:SEAP/Neo vector produced in Example 31, EGR1 amplified product can then be inserted into this vector. Linearize the GAS:SEAP/Neo vector using restriction enzymes XhoI/HindIII, removing the GAS/SV40 stuffer. Restrict the EGR1 amplified product with these same enzymes. Ligate the vector and the EGR1 promoter.

To prepare 96 well-plates for cell culture, two mls of a coating solution (1:30 dilution of collagen type I (Upstate Biotech Inc. Cat#08-115) in 30% ethanol (filter sterilized)) is added per one 10 cm plate or 50 ml per well of the 96-well plate, and allowed to air dry for 2 hr.

PC12 cells are routinely grown in RPMI-1640 medium (Bio Whittaker) containing 10% horse serum (JRH BIOSCIENCES, Cat. # 12449-78P), 5% heat-inactivated fetal bovine serum (FBS) supplemented with 100 units/ml penicillin and 100 ug/ml streptomycin on a precoated 10 cm tissue culture dish. One to four split is done every three to four days. Cells are removed from the plates by scraping and resuspended with pipetting up and down for more than 15 times.

Transfect the EGR/SEAP/Neo construct into PC12 using the Lipofectamine protocol described in Example 30. EGR-SEAP/PC12 stable cells are obtained by growing the cells in 300 ug/ml G418. The G418-free medium is used for routine growth but every one to two months, the cells should be re-grown in 300 ug/ml G418 for couple of passages.

To assay for neuronal activity, a 10 cm plate with cells around 70 to 80% confluent is screened by removing the old medium. Wash the cells once with PBS (Phosphate buffered saline). Then starve the cells in low serum medium (RPMI-1640 containing 1% horse serum and 0.5% FBS with antibiotics) overnight.

The next morning, remove the medium and wash the cells with PBS. Scrape off the cells from the plate, suspend the cells well in 2 ml low serum medium. Count the cell number and add more low serum medium to reach final cell density as 5×10⁵ cells/ml.

Add 200 ul of the cell suspension to each well of 96-well plate (equivalent to 1×10⁵ cells/well). Add 50 ul supernatant produced by Example 30, 37 degree C. for 48 to 72 hr. As a positive control, a growth factor known to activate PC12 cells through EGR can be used, such as 50 ng/ul of Neuronal Growth Factor (NGF). Over fifty-fold induction of SEAP is typically seen in the positive control wells. SEAP assay the supernatant according to Example 36.

Example 35 High-Throughput Screening Assay for T-Cell Activity

NF-KB (Nuclear Factor KB) is a transcription factor activated by a wide variety of agents including the inflammatory cytokines IL-1 and TNF, CD30 and CD40, lymphotoxin-alpha and lymphotoxin-beta, by exposure to LPS or thrombin, and by expression of certain viral gene products. As a transcription factor, NF-KB regulates the expression of genes involved in immune cell activation, control of apoptosis (F— KB appears to shield cells from apoptosis), B and T-cell development, anti-viral and antimicrobial responses, and multiple stress responses.

In non-stimulated conditions, NF-KB is retained in the cytoplasm with I-KB (Inhibitor KB). However, upon stimulation, I— KB is phosphorylated and degraded, causing NF-KB to shuttle to the nucleus, thereby activating transcription of target genes. Target genes activated by NF-KB include IL-2, IL-6, GM-CSF, ICAM-1 and class 1 MHC.

Due to its central role and ability to respond to a range of stimuli, reporter constructs utilizing the NF-KB promoter element are used to screen the supernatants produced in Example 30. Activators or inhibitors of NF-KB would be useful in detecting, preventing, diagnosing, prognosticating, treating, and/or ameliorating diseases. For example, inhibitors of NF-KB could be used to treat those diseases related to the acute or chronic activation of NF-KB, such as rheumatoid arthritis.

To construct a vector containing the NF-KB promoter element, a PCR based strategy is employed. The upstream primer contains four tandem copies of the NF-KB binding site (GGGGACTTTCCC) (SEQ ID NO: 8), 18 bp of sequence complementary to the 5′ end of the SV40 early promoter sequence, and is flanked with an XhoI site: (SEQ ID NO:9) 5′:GCGGCCTCGAGGGGACTTTCCCGGGGACTTTCCGGGGACTTTCCGGG ACTTTCCATCCTGCCATCTCAATTAG:3′

The downstream primer is complementary to the 3′ end of the SV40 promoter and is flanked with a Hind III site: (SEQ ID NO:4) 5′:GCGGCAAGCTTTTTGCAAAGCCTAGGC:3′

PCR amplification is performed using the SV40 promoter template present in the pB-gal:promoter plasmid obtained from CLONTECH™. The resulting PCR fragment is digested with XhoI and Hind III and subcloned into BLSK2-. (STRATAGENE™) Sequencing with the T7 and T3 primers confirms the insert contains the following sequence: (SEQ ID NO:10) 5′:CTCGAGGGGACTTTCCCGGGGACTTTCCGGGGACTTTCCGGGACTTT CCATCTGCCATCTCAATTAGTCAGCAACCATAGTCCCGCCCCTAACTCCG CCCATCCCGCCCCTAACTCCGCCCAGTTCCGCCCATTCTCCGCCCCATGG CTGACTAATTTTTTTTATTTATGCAGAGGCCGAGGCCGCCTCGGCCTCTG AGCTATTCCAGAAGTAGTGAGGAGGCTTTTTTGGAGGCCTAGGCTTTTGC AAAAAGCTT:3′

Next, replace the SV40 minimal promoter element present in the pSEAP2-promoter plasmid (CLONTECH™) with this NF-KB/SV40 fragment using XhoI and HindIII. However, this vector does not contain a neomycin resistance gene, and therefore, is not preferred for mammalian expression systems.

In order to generate stable mammalian cell lines, the NF-KB/SV40/SEAP cassette is removed from the above NF-KB/SEAP vector using restriction enzymes SalI and NotI, and inserted into a vector containing neomycin resistance. Particularly, the NF-KB/SV40/SEAP cassette was inserted into pGFP-1 (CLONTECH™), replacing the GFP gene, after restricting pGFP-1 with SalI and NotI.

Once NF-KB/SV40/SEAP/Neo vector is created, stable Jurkat T-cells are created and maintained according to the protocol described in Example 32. Similarly, the method for assaying supernatants with these stable Jurkat T-cells is also described in Example 32. As a positive control, exogenous TNF alpha (0.1, 1, 10 ng) is added to wells H9, H10, and H11, with a 5-10 fold activation typically observed.

Example 36 Assay for SEAP Activity

As a reporter molecule for the assays described in Examples 32-35, SEAP activity is assayed using the Tropix Phospho-light Kit (Cat. BP-400) according to the following general procedure. The Tropix Phospho-light Kit supplies the Dilution, Assay, and Reaction Buffers used below.

Prime a dispenser with the 2.5× Dilution Buffer and dispense 15 ul of 2.5× dilution buffer into Optiplates containing 35 ul of a supernatant. Seal the plates with a plastic sealer and incubate at 65 degree C. for 30 min. Separate the Optiplates to avoid uneven heating.

Cool the samples to room temperature for 15 minutes. Empty the dispenser and prime with the Assay Buffer. Add 50 ml Assay Buffer and incubate at room temperature 5 min. Empty the dispenser and prime with the Reaction Buffer (see the Table below). Add 50 ul Reaction Buffer and incubate at room temperature for 20 minutes. Since the intensity of the chemiluminescent signal is time dependent, and it takes about 10 minutes to read 5 plates on a luminometer, thus one should treat 5 plates at each time and start the second set 10 minutes later.

Read the relative light unit in the luminometer. Set H12 as blank, and print the results. An increase in chemiluminescence indicates reporter activity. Reaction Buffer Formulation: # of plates Rxn buffer diluent (ml) CSPD (ml) 10 60 3 11 65 3.25 12 70 3.5 13 75 3.75 14 80 4 15 85 4.25 16 90 4.5 17 95 4.75 18 100 5 19 105 5.25 20 110 5.5 21 115 5.75 22 120 6 23 125 6.25 24 130 6.5 25 135 6.75 26 140 7 27 145 7.25 28 150 7.5 29 155 7.75 30 160 8 31 165 8.25 32 170 8.5 33 175 8.75 34 180 9 35 185 9.25 36 190 9.5 37 195 9.75 38 200 10 39 205 10.25 40 210 10.5 41 215 10.75 42 220 11 43 225 11.25 44 230 11.5 45 235 11.75 46 240 12 47 245 12.25 48 250 12.5 49 255 12.75 50 260 13

Example 37 High-Throughput Screening Assay Identifying Changes in Small Molecule Concentration and Membrane Permeability

Binding of a ligand to a receptor is known to alter intracellular levels of small molecules, such as calcium, potassium, sodium, and pH, as well as alter membrane potential. These alterations can be measured in an assay to identify supernatants which bind to receptors of a particular cell. Although the following protocol describes an assay for calcium, this protocol can easily be modified to detect changes in potassium, sodium, pH, membrane potential, or any other small molecule which is detectable by a fluorescent probe.

The following assay uses Fluorometric Imaging Plate Reader (“FLIPR”) to measure changes in fluorescent molecules (Molecular Probes) that bind small molecules. Clearly, any fluorescent molecule detecting a small molecule can be used instead of the calcium fluorescent molecule, fluo-4 (Molecular Probes, Inc.; catalog no. F-14202), used here.

For adherent cells, seed the cells at 10,000-20,000 cells/well in a Co-star black 96-well plate with clear bottom. The plate is incubated in a CO₂ incubator for 20 hours. The adherent cells are washed two times in Biotek washer with 200 ul of HBSS (Hank's Balanced Salt Solution) leaving 100 ul of buffer after the final wash.

A stock solution of 1 mg/ml fluo-4 is made in 10% pluronic acid DMSO. To load the cells with fluo-4, 50 ul of 12 ug/ml fluo-4 is added to each well. The plate is incubated at 37 degrees C. in a CO₂ incubator for 60 min. The plate is washed four times in the Biotek washer with HBSS leaving 100 ul of buffer.

For non-adherent cells, the cells are spun down from culture media. Cells are re-suspended to 2-5×10⁶ cells/ml with HBSS in a 50-ml conical tube. 4 ul of 1 mg/ml fluo-4 solution in 10% pluronic acid

DMSO is added to each ml of cell suspension. The tube is then placed in a 37 degrees C. water bath for 30-60 min. The cells are washed twice with HBSS, resuspended to 1×10⁶ cells/ml, and dispensed into a microplate, 100 ul/well. The plate is centrifuged at 1000 rpm for 5 min. The plate is then washed once in Denley Cell Wash with 200 ul, followed by an aspiration step to 100 ul final volume.

For a non-cell based assay, each well contains a fluorescent molecule, such as fluo-4. The supernatant is added to the well, and a change in fluorescence is detected.

To measure the fluorescence of intracellular calcium, the FLIPR is set for the following parameters: (1) System gain is 300-800 mW; (2) Exposure time is 0.4 second; (3) Camera F/stop is F/2; (4) Excitation is 488 nm; (5) Emission is 530 nm; and (6) Sample addition is 50 ul. Increased emission at 530 nm indicates an extracellular signaling event caused by the a molecule, either polypeptide of the present invention or a molecule induced by polypeptide of the present invention, which has resulted in an increase in the intracellular Ca⁺⁺ concentration.

Example 38 High-Throughput Screening Assay Identifying Tyrosine Kinase Activity

The Protein Tyrosine Kinases (PTK) represent a diverse group of transmembrane and cytoplasmic kinases. Within the Receptor Protein Tyrosine Kinase RPTK) group are receptors for a range of mitogenic and metabolic growth factors including the PDGF, FGF, EGF, NGF, HGF and Insulin receptor subfamilies. In addition there are a large family of RPTKs for which the corresponding ligand is unknown. Ligands for RPTKs include mainly secreted small proteins, but also membrane-bound and extracellular matrix proteins.

Activation of RPTK by ligands involves ligand-mediated receptor dimerization, resulting in transphosphorylation of the receptor subunits and activation of the cytoplasmic tyrosine kinases. The cytoplasmic tyrosine kinases include receptor associated tyrosine kinases of the src-family (e.g., src, yes, lck, lyn, fyn) and non-receptor linked and cytosolic protein tyrosine kinases, such as the Jak family, members of which mediate signal transduction triggered by the cytokine superfamily of receptors (e.g., the Interleukins, Interferons, GM-CSF, and Leptin).

Because of the wide range of known factors capable of stimulating tyrosine kinase activity, identifying whether polypeptide of the present invention or a molecule induced by polypeptide of the present invention is capable of activating tyrosine kinase signal transduction pathways is of interest. Therefore, the following protocol is designed to identify such molecules capable of activating the tyrosine kinase signal transduction pathways.

Seed target cells (e.g., primary keratinocytes) at a density of approximately 25,000 cells per well in a 96 well LOPRODYNE™ Silent Screen Plates purchased from Nalge Nunc (Naperville, Ill.). The plates are sterilized with two 30 minute rinses with 100% ethanol, rinsed with water and dried overnight. Some plates are coated for 2 hr with 100 ml of cell culture grade type I collagen (50 mg/ml), gelatin (2%) or polylysine (50 mg/ml), all of which can be purchased from SIGMA™ Chemicals (St. Louis, Mo.) or 10% MATRIGEL™ purchased from Becton Dickinson (Bedford, Mass.), or calf serum, rinsed with PBS and stored at 4 degree C. Cell growth on these plates is assayed by seeding 5,000 cells/well in growth medium and indirect quantitation of cell number through use of ALAMAR BLUE™ as described by the manufacturer Alamar Biosciences, Inc. (Sacramento, Calif.) after 48 hr. Falcon plate covers #3071 from Becton Dickinson (Bedford, Mass.) are used to cover the LOPRODYNE™ Silent Screen Plates. Falcon Microtest III cell culture plates can also be used in some proliferation experiments.

To prepare extracts, A431 cells are seeded onto the nylon membranes of LOPRODYNE™ plates (20,000/200 ml/well) and cultured overnight in complete medium. Cells are quiesced by incubation in serum-free basal medium for 24 hr. After 5-20 minutes treatment with EGF (60 ng/ml) or 50 ul of the supernatant produced in Example 30, the medium was removed and 100 ml of extraction buffer ((20 mM HEPES pH 7.5, 0.15 M NaCl, 1% Triton X-100, 0.1% SDS, 2 mM Na3VO4, 2 mM Na4P2O7 and a cocktail of protease inhibitors (# 1836170) obtained from Boeheringer Mannheim (Indianapolis, Ind.)) is added to each well and the plate is shaken on a rotating shaker for 5 minutes at 4° C. The plate is then placed in a vacuum transfer manifold and the extract filtered through the 0.45 mm membrane bottoms of each well using house vacuum. Extracts are collected in a 96-well catch/assay plate in the bottom of the vacuum manifold and immediately placed on ice. To obtain extracts clarified by centrifugation, the content of each well, after detergent solubilization for 5 minutes, is removed and centrifuged for 15 minutes at 4 degree C. at 16,000×g.

Test the filtered extracts for levels of tyrosine kinase activity. Although many methods of detecting tyrosine kinase activity are known, one method is described here.

Generally, the tyrosine kinase activity of a supernatant is evaluated by determining its ability to phosphorylate a tyrosine residue on a specific substrate (a biotinylated peptide). Biotinylated peptides that can be used for this purpose include PSK1 (corresponding to amino acids 6-20 of the cell division kinase cdc2-p34) and PSK2 (corresponding to amino acids 1-17 of gastrin). Both peptides are substrates for a range of tyrosine kinases and are available from BOEHRINGER™ Mannheim.

The tyrosine kinase reaction is set up by adding the following components in order. First, add 10 ul of 5 uM Biotinylated Peptide, then 10 ul ATP/Mg₂₊ (5 mM ATP/50 mM MgCl₂), then 10 ul of 5× Assay Buffer (40 mM imidazole hydrochloride, pH7.3, 40 mM beta-glycerophosphate, 1 mM EGTA, 100 mM MgCl₂, 5 mM MnCl₂, 0.5 mg/ml BSA), then 5 ul of Sodium Vanadate (1 mM), and then 5 ul of water. Mix the components gently and preincubate the reaction mix at 30 degree C. for 2 min. Initial the reaction by adding 10 ul of the control enzyme or the filtered supernatant.

The tyrosine kinase assay reaction is then terminated by adding 10 ul of 120 mm EDTA and place the reactions on ice.

Tyrosine kinase activity is determined by transferring 50 ul aliquot of reaction mixture to a microtiter plate (MTP) module and incubating at 37 degree C. for 20 min. This allows the streptavidin coated 96 well plate to associate with the biotinylated peptide. Wash the MTP module with 300 ul/well of PBS four times. Next add 75 ul of anti-phosphotyrosine antibody conjugated to horse radish peroxidase(anti-P-Tyr-POD(0.5u/ml)) to each well and incubate at 37 degree C. for one hour. Wash the well as above.

Next add 100 ul of peroxidase substrate solution (BOEHRINGER™ Mannheim) and incubate at room temperature for at least 5 mins (up to 30 min). Measure the absorbance of the sample at 405 nm by using ELISA reader. The level of bound peroxidase activity is quantitated using an ELISA reader and reflects the level of tyrosine kinase activity.

Example 39 High-Throughput Screening Assay Identifying Phosphorylation Activity

As a potential alternative and/or complement to the assay of protein tyrosine kinase activity described in Example 38, an assay which detects activation (phosphorylation) of major intracellular signal transduction intermediates can also be used. For example, as described below one particular assay can detect tyrosine phosphorylation of the Erk-1 and Erk-2 kinases. However, phosphorylation of other molecules, such as Raf, JNK, p38 MAP, Map kinase kinase (MEK), MEK kinase, Src, Muscle specific kinase (MuSK), IRAK, Tec, and Janus, as well as any other phosphoserine, phosphotyrosine, or phosphothreonine molecule, can be detected by substituting these molecules for Erk-1 or Erk-2 in the following assay.

Specifically, assay plates are made by coating the wells of a 96-well ELISA plate with 0.1 ml of protein G (1 ug/ml) for 2 hr at room temp, (RT). The plates are then rinsed with PBS and blocked with 3% BSA/PBS for 1 hr at RT. The protein G plates are then treated with 2 commercial monoclonal antibodies (10 ng/well) against Erk-1 and Erk-2 (1 hr at RT) (Santa Cruz Biotechnology). (To detect other molecules, this step can easily be modified by substituting a monoclonal antibody detecting any of the above described molecules.) After 3-5 rinses with PBS, the plates are stored at 4 degree C. until use.

A431 cells are seeded at 20,000/well in a 96-well LOPRODYNE™ filterplate and cultured overnight in growth medium. The cells are then starved for 48 hr in basal medium (DMEM) and then treated with EGF (6 ng/well) or 50 ul of the supernatants obtained in Example 30 for 5-20 minutes. The cells are then solubilized and extracts filtered directly into the assay plate.

After incubation with the extract for 1 hr at RT, the wells are again rinsed. As a positive control, a commercial preparation of MAP kinase (10 ng/well) is used in place of A431 extract. Plates are then treated with a commercial polyclonal (rabbit) antibody (1 ug/ml) which specifically recognizes the phosphorylated epitope of the Erk-1 and Erk-2 kinases (1 hr at RT). This antibody is biotinylated by standard procedures. The bound polyclonal antibody is then quantitated by successive incubations with Europium-streptavidin and Europium fluorescence enhancing reagent in the Wallac DELFIA instrument (time-resolved fluorescence). An increased fluorescent signal over background indicates a phosphorylation by polypeptide of the present invention or a molecule induced by polypeptide of the present invention.

Example 40 Assay for the Stimulation of Bone Marrow CD34+ Cell Proliferation

This assay is based on the ability of human CD34+ to proliferate in the presence of hematopoietic growth factors and evaluates the ability of isolated polypeptides expressed in mammalian cells to stimulate proliferation of CD34+ cells.

It has been previously shown that most mature precursors will respond to only a single signal. More immature precursors require at least two signals to respond. Therefore, to test the effect of polypeptides on hematopoietic activity of a wide range of progenitor cells, the assay contains a given polypeptide in the presence or absence of other hematopoietic growth factors. Isolated cells are cultured for 5 days in the presence of Stem Cell Factor (SCF) in combination with tested sample. SCF alone has a very limited effect on the proliferation of bone marrow (BM) cells, acting in such conditions only as a “survival” factor. However, combined with any factor exhibiting stimulatory effect on these cells (e.g., IL-3), SCF will cause a synergistic effect. Therefore, if the tested polypeptide has a stimulatory effect on hematopoietic progenitors, such activity can be easily detected. Since normal BM cells have a low level of cycling cells, it is likely that any inhibitory effect of a given polypeptide, or agonists or antagonists thereof, might not be detected. Accordingly, assays for an inhibitory effect on progenitors is preferably tested in cells that are first subjected to in vitro stimulation with SCF+IL+3, and then contacted with the compound that is being evaluated for inhibition of such induced proliferation.

Briefly, CD34+ cells are isolated using methods known in the art. The cells are thawed and resuspended in medium (QBSF 60 serum-free medium with 1% L-glutamine (500 ml) Quality Biological, Inc., Gaithersburg, Md. Cat# 160-204-101). After several gentle centrifugation steps at 200×g, cells are allowed to rest for one hour. The cell count is adjusted to 2.5×10⁵ cells/ml. During this time, 100 μl of sterile water is added to the peripheral wells of a 96-well plate. The cytokines that can be tested with a given polypeptide in this assay is rhSCF (R&D Systems, Minneapolis, Minn., Cat# 255-SC) at 50 ng/ml alone and in combination with rhSCF and rhIL-3 (R&D Systems, Minneapolis, Minn., Cat# 203-ML) at 30 ng/ml. After one hour, 10 μl of prepared cytokines, 50 μl of the supernatants prepared in Example 30 (supernatants at 1:2 dilution=50 μl) and 20 μl of diluted cells are added to the media which is already present in the wells to allow for a final total volume of 100 μl. The plates are then placed in a 37° C./5% CO₂ incubator for five days.

Eighteen hours before the assay is harvested, 0.5 μCi/well of [3H] Thymidine is added in a 10 μl volume to each well to determine the proliferation rate. The experiment is terminated by harvesting the cells from each 96-well plate to a filtermat using the Tomtec Harvester 96. After harvesting, the filtermats are dried, trimmed and placed into OMNIFILTER™ assemblies consisting of one OMNIFILTER™ plate and one OMNIFILTER™ Tray. 60 μl MICROSCINT™ is added to each well and the plate sealed with TopSeal-A press-on sealing film A bar code 15 sticker is affixed to the first plate for counting. The sealed plates are then loaded and the level of radioactivity determined via the Packard Top Count and the printed data collected for analysis. The level of radioactivity reflects the amount of cell proliferation.

The studies described in this example test the activity of a given polypeptide to stimulate bone marrow CD34+ cell proliferation. One skilled in the art could easily modify the exemplified studies to test the activity of polynucleotides (e.g., gene therapy), antibodies, agonists, and/or antagonists and fragments and variants thereof. As a nonlimiting example, potential antagonists tested in this assay would be expected to inhibit cell proliferation in the presence of cytokines and/or to increase the inhibition of cell proliferation in the presence of cytokines and a given polypeptide. In contrast, potential agonists tested in this assay would be expected to enhance cell proliferation and/or to decrease the inhibition of cell proliferation in the presence of cytokines and a given polypeptide.

The ability of a gene to stimulate the proliferation of bone marrow CD34+ cells indicates that polynucleotides and polypeptides corresponding to the gene are useful for the detection, prevention, diagnosis, prognostication, treatment, and/or amelioration of disorders affecting the immune system and hematopoiesis. Representative uses are described in the “Immune Activity” and “Infectious Disease” sections above, and elsewhere herein.

Example 41 Assay for Extracellular Matrix Enhanced Cell Response (EMECR)

The objective of the Extracellular Matrix Enhanced Cell Response (EMECR) assay is to identify gene products (e.g., isolated polypeptides) that act on the hematopoietic stem cells in the context of the extracellular matrix (ECM) induced signal.

Cells respond to the regulatory factors in the context of signal(s) received from the surrounding microenvironment. For example, fibroblasts, and endothelial and epithelial stem cells fail to replicate in the absence of signals from the ECM. Hematopoietic stem cells can undergo self-renewal in the bone marrow, but not in in vitro suspension culture. The ability of stem cells to undergo self-renewal in vitro is dependent upon their interaction with the stromal cells and the ECM protein fibronectin (fn). Adhesion of cells to fn is mediated by the α₅.β₁ and α₄.β₁ integrin receptors, which are expressed by human and mouse hematopoietic stem cells. The factor(s) which integrate with the ECM environment and are responsible for stimulating stem cell self-renewal have a not yet been identified. Discovery of such factors should be of great interest in gene therapy and bone marrow transplant applications

Briefly, polystyrene, non tissue culture treated, 96-well plates are coated with fn fragment at a coating concentration of 0.2 μg/cm². Mouse bone marrow cells are plated (1,000 cells/well) in 0.2 ml of serum-free medium. Cells cultured in the presence of IL-3 (5 ng/ml)+SCF (50 ng/ml) would serve as the positive control, conditions under which little self-renewal but pronounced differentiation of the stem cells is to be expected. Gene products of the invention (e.g., including, but not limited to, polynucleotides and polypeptides of the present invention, and supernatants produced in Example 30), are tested with appropriate negative controls in the presence and absence of SCF (5.0 ng/ml), where test factor supernatants represent 10% of the total assay volume. The plated cells are then allowed to grow by incubating in a low oxygen environment (5% CO₂, 7% O₂, and 88% N₂) tissue culture incubator for 7 days. The number of proliferating cells within the wells is then quantitated by measuring thymidine incorporation into cellular DNA. Verification of the positive hits in the assay will require phenotypic characterization of the cells, which can be accomplished by scaling up of the culture system and using appropriate antibody reagents against cell surface antigens and FACScan.

One skilled in the art could easily modify the exemplified studies to test the activity of polynucleotides (e.g., gene therapy), antibodies, agonists, and/or antagonists and fragments and variants thereof.

If a particular polypeptide of the present invention is found to be a stimulator of hematopoietic progenitors, polynucleotides and polypeptides corresponding to the gene encoding said polypeptide may be useful for the detection, prevention, diagnosis, prognostication, treatment, and/or amelioration of disorders affecting the immune system and hematopoiesis. Representative uses are described in the “Immune Activity” and “Infectious Disease” sections above, and elsewhere herein. The gene product may also be useful in the expansion of stem cells and committed progenitors of various blood lineages, and in the differentiation and/or proliferation of various cell types.

Additionally, the polynucleotides and/or polypeptides of the gene of interest and/or agonists and/or antagonists thereof, may also be employed to inhibit the proliferation and differentiation of hematopoietic cells and therefore may be employed to protect bone marrow stem cells from chemotherapeutic agents during chemotherapy. This antiproliferative effect may allow administration of higher doses of chemotherapeutic agents and, therefore, more effective chemotherapeutic treatment.

Moreover, polynucleotides and polypeptides corresponding to the gene of interest may also be useful for the detection, prevention, diagnosis, prognostication, treat, and/or amelioration of hematopoietic related disorders such as, for example, anemia, pancytopenia, leukopenia, thrombocytopenia or leukemia since stromal cells are important in the production of cells of hematopoietic lineages. The uses include bone marrow cell ex-vivo culture, bone marrow transplantation, bone marrow reconstitution, radiotherapy or chemotherapy of neoplasia.

Example 42 Human Dermal Fibroblast and Aortic Smooth Muscle Cell Proliferation

The polypeptide of interest is added to cultures of normal human dermal fibroblasts (HDF) and human aortic smooth muscle cells (AoSMC) and two co-assays are performed with each sample. The first assay examines the effect of the polypeptide of interest on the proliferation of normal human dermal fibroblasts (NHDF) or aortic smooth muscle cells (AoSMC). Aberrant growth of fibroblasts or smooth muscle cells is a part of several pathological processes, including fibrosis, and restenosis. The second assay examines IL6 production by both NHDF and SMC. IL6 production is an indication of functional activation. Activated cells will have increased production of a number of cytokines and other factors, which can result in a proinflammatory or immunomodulatory outcome. Assays are run with and without co-TNFa stimulation, in order to check for costimulatory or inhibitory activity.

Briefly, on day 1, 96-well black plates are set up with 1000 cells/well (HDF) or 2000 cells/well (AoSMC) in 100 μl culture media. NHDF culture media contains: Clonetics FB basal media, 1 mg/ml hFGF, 5 mg/ml insulin, 50 mg/ml gentamycin, 2% FBS, while AoSMC culture media contains Clonetics SM basal media, 0.5 pg/ml hEGF, 5 mg/ml insulin, 1 μg/ml hFGF, 50 mg/ml gentamycin, 50 pg/ml Amphotericin B, 5% FBS. After incubation at 37° C. for at least 4-5 hours culture media is aspirated and replaced with growth arrest media. Growth arrest media for NHDF contains fibroblast basal media, 50 mg/ml gentamycin, 2% FBS, while growth arrest media for AoSMC contains SM basal media, 50 mg/ml gentamycin, 50 pg/ml Amphotericin B, 0.4% FBS. Incubate at 37° C. until day 2.

On day 2, serial dilutions and templates of the polypeptide of interest are designed such that they always include media controls and known-protein controls. For both stimulation and inhibition experiments, proteins are diluted in growth arrest media. For inhibition experiments, TNFa is added to a final concentration of 2 ng/ml (HDF) or 5 ng/ml (AoSMC). Add ⅓ vol media containing controls or polypeptides of the present invention and incubate at 37 degrees C./5% CO₂ until day 5.

Transfer 60 μl from each well to another labeled 96-well plate, cover with a plate-sealer, and store at 4 degrees C. until Day 6 (for IL6 ELISA). To the remaining 100 μl in the cell culture plate, aseptically add ALAMAR BLUE™ in an amount equal to 10% of the culture volume (10 μl). Return plates to incubator for 3 to 4 hours. Then measure fluorescence with excitation at 530 nm and emission at 590 nm using the CYTOFLUOR™. This yields the growth stimulation/inhibition data.

On day 5, the IL6 ELISA is performed by coating a 96 well plate with 50-100 ul/well of Anti-Human IL6 Monoclonal antibody diluted in PBS, pH 7.4, incubate ON at room temperature.

On day 6, empty the plates into the sink and blot on paper towels. Prepare Assay Buffer containing PBS with 4% BSA. Block the plates with 200 μl/well of Pierce Super Block blocking buffer in PBS for 1-2 hr and then wash plates with wash buffer (PBS, 0.05% Tween-20). Blot plates on paper towels. Then add 50 μl/well of diluted Anti-Human IL-6 Monoclonal, Biotin-labeled antibody at 0.50 mg/ml. Make dilutions of IL-6 stock in media (30, 10, 3, 1, 0.3, 0 ng/ml). Add duplicate samples to top row of plate. Cover the plates and incubate for 2 hours at RT on shaker.

Plates are washed with wash buffer and blotted on paper towels. Dilute EU-labeled Streptavidin 1:1000 in Assay buffer, and add 100 μl/well. Cover the plate and incubate 1 h at RT. Plates are again washed with wash buffer and blotted on paper towels.

Add 100 μl/well of Enhancement Solution. Shake for 5 minutes. Read the plate on the Wallac DELFIA Fluorometer. Readings from triplicate samples in each assay were tabulated and averaged.

A positive result in this assay suggests AoSMC cell proliferation and that the polypeptide of the present invention may be involved in dermal fibroblast proliferation and/or smooth muscle cell proliferation. A positive result also suggests many potential uses of polypeptides, polynucleotides, agonists and/or antagonists of the polynucleotide/polypeptide of the present invention which gives a positive result. For example, inflammation and immune responses, wound healing, and angiogenesis, as detailed throughout this specification. Particularly, polypeptides of the present invention and polynucleotides of the present invention may be used in wound healing and dermal regeneration, as well as the promotion of vasculogenesis, both of the blood vessels and lymphatics. The growth of vessels can be used in the treatment of, for example, cardiovascular diseases. Additionally, antagonists of polypeptides and polynucleotides of the invention may be useful in treating diseases, disorders, and/or conditions which involve angiogenesis by acting as an anti-vascular agent (e.g., anti-angiogenesis). These diseases, disorders, and/or conditions are known in the art and/or are described herein, such as, for example, malignancies, solid tumors, benign tumors, for example hemangiomas, acoustic neuromas, neurofibromas, trachomas, and pyogenic granulomas; artheroscleric plaques; ocular angiogenic diseases, for example, diabetic retinopathy, retinopathy of prematurity, macular degeneration, corneal graft rejection, neovascular glaucoma, retrolental fibroplasia, rubeosis, retinoblastoma, uvietis and Pterygia (abnormal blood vessel growth) of the eye; rheumatoid arthritis; psoriasis; delayed wound healing; endometriosis; vasculogenesis; granulations; hypertrophic scars (keloids); nonunion fractures; scleroderma; trachoma; vascular adhesions; myocardial angiogenesis; coronary collaterals; cerebral collaterals; arteriovenous malformations; ischemic limb angiogenesis; Osler-Webber Syndrome; plaque neovascularization; telangiectasia; hemophiliac joints; angiofibroma; fibromuscular dysplasia; wound granulation; Crohn's disease; and atherosclerosis. Moreover, antagonists of polypeptides and polynucleotides of the invention may be useful in treating anti-hyperproliferative diseases and/or anti-inflammatory known in the art and/or described herein.

One skilled in the art could easily modify the exemplified studies to test the activity of polynucleotides (e.g., gene therapy), antibodies, agonists, and/or antagonists and fragments and variants thereof.

Example 43 Cellular Adhesion Molecule (CAM) Expression on Endothelial Cells

The recruitment of lymphocytes to areas of inflammation and angiogenesis involves specific receptor-ligand interactions between cell surface adhesion molecules (CAMs) on lymphocytes and the vascular endothelium. The adhesion process, in both normal and pathological settings, follows a multi-step cascade that involves intercellular adhesion molecule-1 (ICAM-1), vascular cell adhesion molecule-1 (VCAM-1), and endothelial leukocyte adhesion molecule-1 (E-selectin) expression on endothelial cells (EC). The expression of these molecules and others on the vascular endothelium determines the efficiency with which leukocytes may adhere to the local vasculature and extravasate into the local tissue during the development of an inflammatory response. The local concentration of cytokines and growth factor participate in the modulation of the expression of these CAMs.

Briefly, endothelial cells (e.g., Human Umbilical Vein Endothelial cells (HUVECs)) are grown in a standard 96 well plate to confluence, growth medium is removed from the cells and replaced with 100 μl of 199 Medium (10% fetal bovine serum (FBS)). Samples for testing and positive or negative controls are added to the plate in triplicate (in 10 μl volumes). Plates are then incubated at 37° C. for either 5 h (selectin and integrin expression) or 24 h (integrin expression only). Plates are aspirated to remove medium and 100 μl of 0.1% paraformaldehyde-PBS(with Ca++ and Mg++) is added to each well. Plates are held at 4° C. for 30 min. Fixative is removed from the wells and wells are washed 1× with PBS(+Ca,Mg)+0.5% BSA and drained. 10 μl of diluted primary antibody is added to the test and control wells. Anti-ICAM-1-Biotin, Anti-VCAM-1-Biotin and Anti-E-selectin-Biotin are used at a concentration of 10 pg/ml (1:10 dilution of 0.1 mg/ml stock antibody). Cells are incubated at 37° C. for 30 min. in a humidified environment. Wells are washed three times with PBS(+Ca,Mg)+0.5% BSA. 20 μl of diluted EXTRAVIDIN™-Alkaline Phosphatase (1:5,000 dilution, referred to herein as the working dilution) are added to each well and incubated at 37° C. for 30 min. Wells are washed three times with PBS(+Ca,Mg)+0.5% BSA. Dissolve 1 tablet of p-Nitrophenol Phosphate pNPP per 5 ml of glycine buffer (pH 10.4). 100 μl of pNPP substrate in glycine buffer is added to each test well. Standard wells in triplicate are prepared from the working dilution of the EXTRAVIDIN™-Alkaline Phosphotase in glycine buffer: 1:5,000 (10⁰)>10^(−0.5)>10⁻¹>10^(−1.5) 0.5 μl of each dilution is added to triplicate wells and the resulting AP content in each well is 5.50 ng, 1.74 ng, 0.55 ng, 0.18 ng. 100 μl of pNNP reagent is then added to each of the standard wells. The plate is incubated at 37° C. for 4 h. A volume of 50 μl of 3M NaOH is added to all wells. The plate is read on a plate reader at 405 nm using the background subtraction option on blank wells filled with glycine buffer only. Additionally, the template is set up to indicate the concentration of AP-conjugate in each standard well [5.50 ng; 1.74 ng; 0.55 ng; 0.18 ng]. Results are indicated as amount of bound AP-conjugate in each sample.

Example 44 ALAMAR BLUE™ Endothelial Cells Proliferation Assay

This assay may be used to quantitatively determine protein mediated inhibition of bFGF-induced proliferation of Bovine Lymphatic Endothelial Cells (LECs), Bovine Aortic Endothelial Cells (BAECs) or Human Microvascular Uterine Myometrial Cells (UTMECs). This assay incorporates a fluorometric growth indicator based on detection of metabolic activity. A standard ALAMAR BLUE™ Proliferation Assay is prepared in EGM-2MV with 10 ng/ml of bFGF added as a source of endothelial cell stimulation. This assay may be used with a variety of endothelial cells with slight changes in growth medium and cell concentration. Dilutions of the protein batches to be tested are diluted as appropriate. Serum-free medium (GIBCO SFM) without bFGF is used as a non-stimulated control and Angiostatin or TSP-1 are included as a known inhibitory controls.

Briefly, LEC, BAECs or UTMECs are seeded in growth media at a density of 5000 to 2000 cells/well in a 96 well plate and placed at 37 degrees C. overnight. After the overnight incubation of the cells, the growth media is removed and replaced with GIBCO EC-SFM. The cells are treated with the appropriate dilutions of the protein of interest or control protein sample(s) (prepared in SFM) in triplicate wells with additional bFGF to a concentration of 10 ng/ml. Once the cells have been treated with the samples, the plate(s) is/are placed back in the 37° C. incubator for three days. After three days 10 ml of stock ALAMAR BLUE™ (Biosource Cat# DAL 1100) is added to each well and the plate(s) is/are placed back in the 37° C. incubator for four hours. The plate(s) are then read at 530 nm excitation and 590 nm emission using the CYTOFLUOR™ fluorescence reader. Direct output is recorded in relative fluorescence units.

ALAMAR BLUE™ is an oxidation-reduction indicator that both fluoresces and changes color in response to chemical reduction of growth medium resulting from cell growth. As cells grow in culture, innate metabolic activity results in a chemical reduction of the immediate surrounding environment. Reduction related to growth causes the indicator to change from oxidized (non-fluorescent blue) form to reduced (fluorescent red) form (i.e., stimulated proliferation will produce a stronger signal and inhibited proliferation will produce a weaker signal and the total signal is proportional to the total number of cells as well as their metabolic activity). The background level of activity is observed with the starvation medium alone. This is compared to the output observed from the positive control samples (bFGF in growth medium) and protein dilutions.

Example 45 Detection of Inhibition of a Mixed Lymphocyte Reaction

This assay can be used to detect and evaluate inhibition of a Mixed Lymphocyte Reaction (MLR) by gene products (e.g., isolated polypeptides). Inhibition of a MLR may be due to a direct effect on cell proliferation and viability, modulation of costimulatory molecules on interacting cells, modulation of adhesiveness between lymphocytes and accessory cells, or modulation of cytokine production by accessory cells. Multiple cells may be targeted by these polypeptides since the peripheral blood mononuclear fraction used in this assay includes T, B and natural killer lymphocytes, as well as monocytes and dendritic cells.

Polypeptides of interest found to inhibit the MLR may find application in diseases associated with lymphocyte and monocyte activation or proliferation. These include, but are not limited to, diseases such as asthma, arthritis, diabetes, inflammatory skin conditions, psoriasis, eczema, systemic lupus erythematosus, multiple sclerosis, glomerulonephritis, inflammatory bowel disease, crohn's disease, ulcerative colitis, arteriosclerosis, cirrhosis, graft vs. host disease, host vs. graft disease, hepatitis, leukemia and lymphoma.

Briefly, PBMCs from human donors are purified by density gradient centrifugation using Lymphocyte Separation Medium (LSM®, density 1.0770 g/ml, Organon Teknika Corporation, West Chester, Pa.). PBMCs from two donors are adjusted to 2×10⁶ cells/ml in RPMI-1640 (LIFE TECHNOLOGIES™, Grand Island, N.Y.) supplemented with 10% FCS and 2 mM glutamine. PBMCs from a third donor is adjusted to 2×10⁵ cells/ml. Fifty microliters of PBMCs from each donor is added to wells of a 96-well round bottom microtiter plate. Dilutions of test materials (50 μl) is added in triplicate to microtiter wells. Test samples (of the protein of interest) are added for final dilution of 1:4; rhuIL-2 (R&D Systems, Minneapolis, Minn., catalog number 202-IL) is added to a final concentration of 1 μg/ml; anti-CD4 mAb (R&D Systems, clone 34930.11, catalog number MAB379) is added to a final concentration of 10 pg/ml. Cells are cultured for 7-8 days at 37° C. in 5% CO₂, and 1 μC of [³H]thymidine is added to wells for the last 16 hrs of culture. Cells are harvested and thymidine incorporation determined using a Packard TopCount. Data is expressed as the mean and standard deviation of triplicate determinations.

Samples of the protein of interest are screened in separate experiments and compared to the negative control treatment, anti-CD4 mAb, which inhibits proliferation of lymphocytes and the positive control treatment, IL-2 (either as recombinant material or supernatant), which enhances proliferation of lymphocytes.

One skilled in the art could easily modify the exemplified studies to test the activity of polynucleotides (e.g., gene therapy), antibodies, agonists, and/or antagonists and fragments and variants thereof.

Example 46 Assays for Protease Activity

The following assay may be used to assess protease activity of the polypeptides of the invention.

Gelatin and casein zymography are performed essentially as described (Heusen et al., Anal. Biochem., 102:196-202 (1980); Wilson et al., Journal of Urology, 149:653-658 (1993)). Samples are run on 10% polyacryamide/0.1% SDS gels containing 1% gelain orcasein, soaked in 2.5% triton at room temperature for 1 hour, and in 0.1M glycine, pH 8.3 at 37° C. 5 to 16 hours. After staining in amido black areas of proteolysis appear as clear areas agains the blue-black background. Trypsin (SIGMA™ T8642) is used as a positive control.

Protease activity is also determined by monitoring the cleavage of n-a-benzoyl-L-arginine ethyl ester (BAEE) (SIGMA™ B-4500. Reactions are set up in (25 mMNaPO₄, 1 mM EDTA, and 1 mM BAEE), pH 7.5. Samples are added and the change in absorbance at 260 nm is monitored on the Beckman DU-6 spectrophotometer in the time-drive mode. Trypsin is used as a positive control.

Additional assays based upon the release of acid-soluble peptides from casein or hemoglobin measured as absorbance at 280 nm or colorimetrically using the Folin method are performed as described in Bergmeyer, et al., Methods of Enzymatic Analysis, 5 (1984). Other assays involve the solubilization of chromogenic substrates (Ward, Applied Science, 251-317 (1983)).

Example 47 Identifying Serine Protease Substrate Specificity

Methods known in the art or described herein may be used to determine the substrate specificity of the polypeptides of the present invention having serine protease activity. A preferred method of determining substrate specificity is by the use of positional scanning synthetic combinatorial libraries as described in GB 2 324 529 (incorporated herein in its entirety).

Example 48 Ligand Binding Assays

The following assay may be used to assess ligand binding activity of the polypeptides of the invention.

Ligand binding assays provide a direct method for ascertaining receptor pharmacology and are adaptable to a high throughput format. The purified ligand for a polypeptide is radiolabeled to high specific activity (50-2000 Ci/mmol) for binding studies. A determination is then made that the process of radiolabeling does not diminish the activity of the ligand towards its polypeptide. Assay conditions for buffers, ions, pH and other modulators such as nucleotides are optimized to establish a workable signal to noise ratio for both membrane and whole cell polypeptide sources. For these assays, specific polypeptide binding is defined as total associated radioactivity minus the radioactivity measured in the presence of an excess of unlabeled competing ligand. Where possible, more than one competing ligand is used to define residual nonspecific binding.

Example 49 Functional Assay in Xenopus Oocytes

Capped RNA transcripts from linearized plasmid templates encoding the polypeptides of the invention are synthesized in vitro with RNA polymerases in accordance with standard procedures. In vitro transcripts are suspended in water at a final concentration of 0.2 mg/ml. Ovarian lobes are removed from adult female toads, Stage V defolliculated oocytes are obtained, and RNA transcripts (10 ng/oocyte) are injected in a 50 nl bolus using a microinjection apparatus. Two electrode voltage clamps are used to measure the currents from individual Xenopus oocytes in response polypeptides and polypeptide agonist exposure. Recordings are made in Ca2+ free Barth's medium at room temperature. The Xenopus system can be used to screen known ligands and tissue/cell extracts for activating ligands.

Example 50 Microphysiometric Assays

Activation of a wide variety of secondary messenger systems results in extrusion of small amounts of acid from a cell. The acid formed is largely as a result of the increased metabolic activity required to fuel the intracellular signaling process. The pH changes in the media surrounding the cell are very small but are detectable by the CYTOSENSOR microphysiometer (Molecular Devices Ltd., Menlo Park, Calif.). The CYTOSENSOR is thus capable of detecting the activation of polypeptide which is coupled to an energy utilizing intracellular signaling pathway.

Example 51 Extract/Cell Supernatant Screening

A large number of mammalian receptors exist for which there remains, as yet, no cognate activating ligand (agonist). Thus, active ligands for these receptors may not be included within the ligands banks as identified to date. Accordingly, the polypeptides of the invention can also be functionally screened (using calcium, cAMP, microphysiometer, oocyte electrophysiology, etc., functional screens) against tissue extracts to identify its natural ligands. Extracts that produce positive functional responses can be sequentially subfractionated until an activating ligand is isolated and identified.

Example 52 Calcium and cAMP Functional Assays

Seven transmembrane receptors which are expressed in HEK 293 cells have been shown to be coupled functionally to activation of PLC and calcium mobilization and/or cAMP stimulation or inhibition. Basal calcium levels in the HEK 293 cells in receptor-transfected or vector control cells were observed to be in the normal, 100 nM to 200 nM, range. HEK 293 cells expressing recombinant receptors are loaded with fura 2 and in a single day >150 selected ligands or tissue/cell extracts are evaluated for agonist induced calcium mobilization. Similarly, HEK 293 cells expressing recombinant receptors are evaluated for the stimulation or inhibition of cAMP production using standard cAMP quantitation assays. Agonists presenting a calcium transient or cAMP fluctuation are tested in vector control cells to determine if the response is unique to the transfected cells expressing receptor.

Example 53 ATP-Binding Assay

The following assay may be used to assess ATP-binding activity of polypeptides of the invention.

ATP-binding activity of the polypeptides of the invention may be detected using the ATP-binding assay described in U.S. Pat. No. 5,858,719, which is herein incorporated by reference in its entirety. Briefly, ATP-binding to polypeptides of the invention is measured via photoaffinity labeling with 8-azido-ATP in a competition assay. Reaction mixtures containing 1 mg/ml of the ABC transport protein of the present invention are incubated with varying concentrations of ATP, or the non-hydrolyzable ATP analog adenyl-5′-imidodiphosphate for 10 minutes at 4° C. A mixture of 8-azido-ATP(SIGMA™ Chem. Corp., St. Louis, Mo.) plus 8-azido-ATP (³²P-ATP) (5 mCi/μmol, ICN, Irvine Calif.) is added to a final concentration of 100 μM and 0.5 ml aliquots are placed in the wells of a porcelain spot plate on ice. The plate is irradiated using a short wave 254 nm UV lamp at a distance of 2.5 cm from the plate for two one-minute intervals with a one-minute cooling interval in between. The reaction is stopped by addition of dithiothreitol to a final concentration of 2 mM. The incubations are subjected to SDS-PAGE electrophoresis, dried, and autoradiographed. Protein bands corresponding to the particular polypeptides of the invention are excised, and the radioactivity quantified. A decrease in radioactivity with increasing ATP or adenly-5′-imidodiphosphate provides a measure of ATP affinity to the polypeptides.

Example 54 Small Molecule Screening

This invention is particularly useful for screening therapeutic compounds by using the polypeptides of the invention, or binding fragments thereof, in any of a variety of drug screening techniques. The polypeptide or fragment employed in such a test may be affixed to a solid support, expressed on a cell surface, free in solution, or located intracellularly. One method of drug screening utilizes eukaryotic or prokaryotic host cells which are stably transformed with recombinant nucleic acids expressing the polypeptide or fragment. Drugs are screened against such transformed cells in competitive binding assays. One may measure, for example, the formulation of complexes between the agent being tested and polypeptide of the invention.

Thus, the present invention provides methods of screening for drugs or any other agents which affect activities mediated by the polypeptides of the invention. These methods comprise contacting such an agent with a polypeptide of the invention or fragment thereof and assaying for the presence of a complex between the agent and the polypeptide or fragment thereof, by methods well known in the art. In such a competitive binding assay, the agents to screen are typically labeled. Following incubation, free agent is separated from that present in bound form, and the amount of free or uncomplexed label is a measure of the ability of a particular agent to bind to the polypeptides of the invention.

Another technique for drug screening provides high throughput screening for compounds having suitable binding affinity to the polypeptides of the invention, and is described in great detail in European Patent Application 84/03564, published on Sep. 13, 1984, which is herein incorporated by reference in its entirety. Briefly stated, large numbers of different small molecule test compounds are synthesized on a solid substrate, such as plastic pins or some other surface. The test compounds are reacted with polypeptides of the invention and washed. Bound polypeptides are then detected by methods well known in the art. Purified polypeptides are coated directly onto plates for use in the aforementioned drug screening techniques. In addition, non-neutralizing antibodies may be used to capture the peptide and immobilize it on the solid support.

This invention also contemplates the use of competitive drug screening assays in which neutralizing antibodies capable of binding polypeptides of the invention specifically compete with a test compound for binding to the polypeptides or fragments thereof. In this manner, the antibodies are used to detect the presence of any peptide which shares one or more antigenic epitopes with a polypeptide of the invention.

Example 55 Phosphorylation Assay

In order to assay for phosphorylation activity of the polypeptides of the invention, a phosphorylation assay as described in U.S. Pat. No. 5,958,405 (which is herein incorporated by reference) is utilized. Briefly, phosphorylation activity may be measured by phosphorylation of a protein substrate using gamma-labeled ³²P-ATP and quantitation of the incorporated radioactivity using a gamma radioisotope counter. The polypeptides of the invention are incubated with the protein substrate, ³²P-ATP, and a kinase buffer. The ³²P incorporated into the substrate is then separated from free ³²P-ATP by electrophoresis, and the incorporated ³²P is counted and compared to a negative control. Radioactivity counts above the negative control are indicative of phosphorylation activity of the polypeptides of the invention.

Example 56 Detection of Phosphorylation Activity (Activation) of the Polypeptides of the Invention in the Presence of Polypeptide Ligands

Methods known in the art or described herein may be used to determine the phosphorylation activity of the polypeptides of the invention. A preferred method of determining phosphorylation activity is by the use of the tyrosine phosphorylation assay as described in U.S. Pat. No. 5,817,471 (incorporated herein by reference).

Example 57 Identification of Signal Transduction Proteins that Interact with Polypeptides of the Present Invention

The purified polypeptides of the invention are research tools for the identification, characterization and purification of additional signal transduction pathway proteins or receptor proteins. Briefly, labeled polypeptides of the invention are useful as reagents for the purification of molecules with which it interacts. In one embodiment of affinity purification, polypeptides of the invention are covalently coupled to a chromatography column. Cell-free extract derived from putative target cells, such as carcinoma tissues, is passed over the column, and molecules with appropriate affinity bind to the polypeptides of the invention. The protein complex is recovered from the column, dissociated, and the recovered molecule subjected to N-terminal protein sequencing. This amino acid sequence is then used to identify the captured molecule or to design degenerate oligonucleotide probes for cloning the relevant gene from an appropriate cDNA library.

Example 58 IL-6 Bioassay

To test the proliferative effects of the polypeptides of the invention, the IL-6 Bioassay as described by Marz et al. is utilized (Proc. Natl. Acad. Sci., U.S.A., 95:3251-56 (1998), which is herein incorporated by reference). Briefly, IL-6 dependent B9 murine cells are washed three times in IL-6 free medium and plated at a concentration of 5,000 cells per well in 50 μl, and 50 μl of the IL-6-like polypeptide is added. After 68 hrs. at 37° C., the number of viable cells is measured by adding the tetrazolium salt thiazolyl blue (MTT) and incubating for a further 4 hrs. at 37° C. B9 cells are lysed by SDS and optical density is measured at 570 nm. Controls containing IL-6 (positive) and no cytokine (negative) are utilized. Enhanced proliferation in the test sample(s) relative to the negative control is indicative of proliferative effects mediated by polypeptides of the invention.

Example 59 Support of Chicken Embryo Neuron Survival

To test whether sympathetic neuronal cell viability is supported by polypeptides of the invention, the chicken embryo neuronal survival assay of Senaldi et al is utilized (Proc. Natl. Acad. Sci., U.S.A., 96:11458-63 (1998), which is herein incorporated by reference). Briefly, motor and sympathetic neurons are isolated from chicken embryos, resuspended in L15 medium (with 10% FCS, glucose, sodium selenite, progesterone, conalbumin, putrescine, and insulin; LIFE TECHNOLOGIES™, Rockville, Md.) and Dulbecco's modified Eagles medium [with 10% FCS, glutamine, penicillin, and 25 mM Hepes buffer (pH 7.2); LIFE TECHNOLOGIES™, Rockville, Md.], respectively, and incubated at 37° C. in 5% CO₂ in the presence of different concentrations of the purified IL-6-like polypeptide, as well as a negative control lacking any cytokine. After 3 days, neuron survival is determined by evaluation of cellular morphology, and through the use of the colorimetric assay of Mosmann (Mosmann, T., J. Immunol. Methods, 65:55-63 (1983)). Enhanced neuronal cell viability as compared to the controls lacking cytokine is indicative of the ability of the inventive purified IL-6-like polypeptide(s) to enhance the survival of neuronal cells.

Example 60 Assay for Phosphatase Activity

The following assay may be used to assess serine/threonine phosphatase (PTPase) activity of the polypeptides of the invention.

In order to assay for serine/threonine phosphatase (PTPase) activity, assays can be utilized which are widely known to those skilled in the art. For example, the serine/threonine phosphatase (PSPase) activity is measured using a PSPase assay kit from New England Biolabs, Inc. Myelin basic protein (MyBP), a substrate for PSPase, is phosphorylated on serine and threonine residues with cAMP-dependent Protein Kinase in the presence of [³²P]ATP. Protein serine/threonine phosphatase activity is then determined by measuring the release of inorganic phosphate from ³²P-labeled MyBP.

Example 61 Interaction of Serine/Threonine Phosphatases with other Proteins

The polypeptides of the invention with serine/threonine phosphatase activity as determined in Example 60 are research tools for the identification, characterization and purification of additional interacting proteins or receptor proteins, or other signal transduction pathway proteins. Briefly, labeled polypeptide(s) of the invention is useful as a reagent for the purification of molecules with which it interacts. In one embodiment of affinity purification, polypeptide of the invention is covalently coupled to a chromatography column. Cell-free extract derived from putative target cells, such as neural or liver cells, is passed over the column, and molecules with appropriate affinity bind to the polypeptides of the invention. The polypeptides of the invention-complex is recovered from the column, dissociated, and the recovered molecule subjected to N-terminal protein sequencing. This amino acid sequence is then used to identify the captured molecule or to design degenerate oligonucleotide probes for cloning the relevant gene from an appropriate cDNA library.

Example 62 Assaying for Heparanase Activity

In order to assay for heparanase activity of the polypeptides of the invention, the heparanase assay described by Vlodavsky et al is utilized (Vlodavsky, I., et al., Nat. Med., 5:793-802 (1999)). Briefly, cell lysates, conditioned media or intact cells (1×10⁶ cells per 35-mm dish) are incubated for 18 hrs at 37° C., pH 6.2-6.6, with ³⁵S-labeled ECM or soluble ECM derived peak I proteoglycans. The incubation medium is centrifuged and the supernatant is analyzed by gel filtration on a Sepharose CL-6B column (0.9×30 cm). Fractions are eluted with PBS and their radioactivity is measured. Degradation fragments of heparan sulfate side chains are eluted from Sepharose 6B at 0.5<K_(av)<0.8 (peak II). Each experiment is done at least three times. Degradation fragments corresponding to “peak II,” as described by Vlodavsky et al., is indicative of the activity of the polypeptides of the invention in cleaving heparan sulfate.

Example 63 Immobilization of Biomolecules

This example provides a method for the stabilization of polypeptides of the invention in non-host cell lipid bilayer constucts (see, e.g., Bieri et al., Nature Biotech 17:1105-1108 (1999), hereby incorporated by reference in its entirety herein) which can be adapted for the study of polypeptides of the invention in the various functional assays described above. Briefly, carbohydrate-specific chemistry for biotinylation is used to confine a biotin tag to the extracellular domain of the polypeptides of the invention, thus allowing uniform orientation upon immobilization. A 50 uM solution of polypeptides of the invention in washed membranes is incubated with 20 mM NaIO4 and 1.5 mg/ml (4 mM) BACH or 2 mg/ml (7.5 mM) biotin-hydrazide for 1 hr at room temperature (reaction volume, 150 ul). Then the sample is dialyzed (Pierce Slidealizer Cassett, 10 kDa cutoff; Pierce Chemical Co., Rockford Ill.) at 4 C first for 5 h, exchanging the buffer after each hour, and finally for 12 h against 500 ml buffer R (0.15 M NaCl, 1 mM MgCl2, 10 mM sodium phosphate, pH7). Just before addition into a cuvette, the sample is diluted 1:5 in buffer ROG50 (Buffer R supplemented with 50 mM octylglucoside).

Example 64 TAQMAN

Quantitative PCR (QPCR). Total RNA from cells in culture are extracted by TRIZOL™ separation as recommended by the supplier (LifeTechnologies). (Total RNA is treated with DNase I (LIFE TECHNOLOGIES™) to remove any contaminating genomic DNA before reverse transcription.) Total RNA (50 ng) is used in a one-step, 50 ul, RT-QPCR, consisting of Taqman Buffer A (Perkin-Elmer; 50 mM KCl/10 mM Tris, pH 8.3), 5.5 mM MgCl₂, 240 μM each dNTP, 0.4 units RNase inhibitor(PROMEGA™), 8% glycerol, 0.012% Tween-20, 0.05% gelatin, 0.3 uM primers, 0.1 uM probe, 0.025 units Amplitaq Gold (Perkin-Elmer) and 2.5 units Superscript II reverse transcriptase (LIFE TECHNOLOGIES™). As a control for genomic contamination, parallel reactions are setup without reverse transcriptase. The relative abundance of (unknown) and 18S RNAs are assessed by using the Applied Biosystems Prism 7700 Sequence Detection System (Livak, K. J., Flood, S. J., Marmaro, J., Giusti, W. & Deetz, K. (1995) PCR Methods Appl. 4, 357-362). Reactions are carried out at 48° C. for 30 min, 95° C. for 10 min, followed by 40 cycles of 95° C. for 15s, 60° C. for 1 min. Reactions are performed in triplicate.

Primers (f & r) and FRET probes sets are designed using Primer Express Software (Perkin-Elmer). Probes are labeled at the 5′-end with the reporter dye 6-FAM and on the 3′-end with the quencher dye TAMRA (Biosource International, Camarillo, Calif. or Perkin-Elmer).

Example 65 Assays for Metalloproteinase Activity

Metalloproteinases (EC 3.4.24.-) are peptide hydrolases which use metal ions, such as Zn²⁺, as the catalytic mechanism. Metalloproteinase activity of polypeptides of the present invention can be assayed according to the following methods.

Proteolysis of alpha-2-macroglobutin

To confirm protease activity, purified polypeptides of the invention are mixed with the substrate alpha-2-macroglobulin (0.2 unit/ml; BOEHRINGER™ Mannheim, Germany) in 1× assay buffer (50 mM HEPES, pH 7.5, 0.2 M NaCl, 10 mM CaCl₂, 25 μM ZnCl₂ and 0.05% Brij-35) and incubated at 37° C. for 1-5 days. Trypsin is used as positive control. Negative controls contain only alpha-2-macroglobulin in assay buffer. The samples are collected and boiled in SDS-PAGE sample buffer containing 5% 2-mercaptoethanol for 5-min, then loaded onto 8% SDS-polyacrylamide gel. After electrophoresis the proteins are visualized by silver staining. Proteolysis is evident by the appearance of lower molecular weight bands as compared to the negative control.

Inhibition of alpha-2-macroglobuin Proteolysis by Inhibitors of Metalloproteinases

Known metalloproteinase inhibitors (metal chelators (EDTA, EGTA, AND HgCl₂), peptide metalloproteinase inhibitors (TIMP-1 and TIMP-2), and commercial small molecule MMP inhibitors) are used to characterize the proteolytic activity of polypeptides of the invention. The three synthetic MMP inhibitors used are: MMP inhibitor I, [IC₅₀=1.0 μM against MMP-1 and MMP-8; IC₅₀=30 μM against MMP-9; IC₅₀=150 μM against MMP-3]; MMP-3 (stromelysin-1) inhibitor I [IC₅₀=5 μM against MMP-3], and MMP-3 inhibitor II [K_(i)=130 nM against MMP-3]; inhibitors available through Calbiochem, catalog #444250, 444218, and 444225, respectively). Briefly, different concentrations of the small molecule MMP inhibitors are mixed with purified polypeptides of the invention (50 pg/ml) in 22.9 μl of 1×HEPES buffer (50 mM HEPES, pH 7.5, 0.2 M NaCl, 10 mM CaCl₂, 25 μM ZnCl₂ and 0.05% Brij-35) and incubated at room temperature (24° C.) for 2-hr, then 7.1 μl of substrate alpha-2-macroglobulin (0.2 unit/ml) is added and incubated at 37° C. for 20-hr. The reactions are stopped by adding 4× sample buffer and boiled immediately for 5 minutes. After SDS-PAGE, the protein bands are visualized by silver stain.

Synthetic Fluorogenic Peptide Substrates Cleavage Assay

The substrate specificity for polypeptides of the invention with demonstrated metalloproteinase activity can be determined using synthetic fluorogenic peptide substrates (purchased from BACHEM Bioscience Inc). Test substrates include, M-1985, M-2225, M-2105, M-2110, and M-2255. The first four are MMP substrates and the last one is a substrate of tumor necrosis factor-α (TNF-α) converting enzyme (TACE). All the substrates are prepared in 1:1 dimethyl sulfoxide (DMSO) and water. The stock solutions are 50-500 μM. Fluorescent assays are performed by using a Perkin Elmer LS 50B luminescence spectrometer equipped with a constant temperature water bath. The excitation λ is 328 nm and the emission λ is 393 nm. Briefly, the assay is carried out by incubating 176 μl 1×HEPES buffer (0.2 M NaCl, 10 mM CaCl₂, 0.05% Brij-35 and 50 mM HEPES, pH 7.5) with 4 μl of substrate solution (50 μM) at 25° C. for 15 minutes, and then adding 20 μl of a purified polypeptide of the invention into the assay cuvett. The final concentration of substrate is 1 μM. Initial hydrolysis rates are monitored for 30-min.

Example 66 Characterization of the cDNA Contained in a Deposited Plasmid

The size of the cDNA insert contained in a deposited plasmid may be routinely determined using techniques known in the art, such as PCR amplification using synthetic primers hybridizable to the 3′ and 5′ ends of the cDNA sequence. For example, two primers of 17-30 nucleotides derived from each end of the cDNA (i.e., hybridizable to the absolute 5′ nucleotide or the 3′ nucleotide end of the sequence of SEQ ID NO:X, respectively) are synthesized and used to amplify the cDNA using the deposited cDNA plasmid as a template. The polymerase chain reaction is carried out under routine conditions, for instance, in 25 ul of reaction mixture with 0.5 ug of the above cDNA template. A convenient reaction mixture is 1.5-5 mM MgCl₂, 0.01% (w/v) gelatin, 20 uM each of DATP, dCTP, dGTP, dTTP, 25 μmol of each primer and 0.25 Unit of Taq polymerase. Thirty five cycles of PCR (denaturation at 94 degree C. for 1 min; annealing at 55 degree C. for 1 min; elongation at 72 degree C. for 1 min) are performed with a Perkin-Elmer Cetus automated thermal cycler. The amplified product is analyzed by agarose gel electrophoresis. The PCR product is verified to be the selected sequence by subcloning and sequencing the DNA product. It will be clear that the invention may be practiced otherwise than as particularly described in the foregoing description and examples. Numerous modifications and variations of the present invention are possible in light of the above teachings and, therefore, are within the scope of the appended claims.

Incorporation by Reference

The entire disclosure of each document cited (including patents, patent applications, journal articles, abstracts, laboratory manuals, books, or other disclosures) in the Background of the Invention, Detailed Description, and Examples is hereby incorporated herein by reference. In addition, the sequence listing submitted herewith is incorporated herein by reference in its entirety. The specification and sequence listing of each of the following U.S. and PCT applications are herein incorporated by reference in their entirety: U.S. Appln. No. 60/040,162 filed on 7 Mar. 1997, U.S. Appln. No. 60/043,576 filed on 11 Apr. 1997, U.S. Appln. No. 60/047,601 filed on 23 May 1997, U.S. Appln. No. 60/056,845 filed on 22 Aug. 1997, U.S. Appln. No. 60/043,580 filed on 11 Apr. 1997, U.S. Appln. No. 60/047,599 filed on 23 May 1997, U.S. Appln. No. 60/056,664 filed on 22 Aug. 1997, U.S. Appln. No. 60/043,314 filed on 11 Apr. 1997, U.S. Appln. No. 60/047,632 filed on 23 May 1997, U.S. Appln. No. 60/056,892 filed on 22 Aug. 1997, U.S. Appln. No. 60/043,568 filed on 11 Apr. 1997, U.S. Appln. No. 60/047,595 filed on 23 May 1997, U.S. Appln. No. 60/056,632 filed on 22 Aug. 1997, U.S. Appln. No. 60/043,578 filed on 11 Apr. 1997, U.S. Appln. No. 60/040,333 filed on 7 Mar. 1997, U.S. Appln. No. 60/043,670 filed on 11 Apr. 1997, U.S. Appln. No. 60/047,596 filed on 23 May 1997, U.S. Appln. No. 60/056,864 filed on 22 Aug. 1997, U.S. Appln. No. 60/043,674 filed on 11 Apr. 1997, U.S. Appln. No. 60/047,612 filed on 23 May 1997, U.S. Appln. No. 60/056,631 filed on 22 Aug. 1997, U.S. Appln. No. 60/043,569 filed on 11 Apr. 1997, U.S. Appln. No. 60/047,588 filed on 23 May 1997, U.S. Appln. No. 60/056,876 filed on 22 Aug. 1997, U.S. Appln. No. 60/043,671 filed on 11 Apr. 1997, U.S. Appln. No. 60/043,311 filed on 11 Apr. 1997, U.S. Appln. No. 60/038,621 filed on 7 Mar. 1997, U.S. Appln. No. 60/043,672 filed on 11 Apr. 1997, U.S. Appln. No. 60/047,613 filed on 23 May 1997, U.S. Appln. No. 60/056,636 filed on 22 Aug. 1997, U.S. Appln. No. 60/043,669 filed on 11 Apr. 1997, U.S. Appln. No. 60/047,582 filed on 23 May 1997, U.S. Appln. No. 60/056,910 filed on 22 Aug. 1997, U.S. Appln. No. 60/043,315 filed on 11 Apr. 1997, U.S. Appln. No. 60/047,598 filed on 23 May 1997, U.S. Appln. No. 60/056,874 filed on 22 Aug. 1997, U.S. Appln. No. 60/043,312 filed on 11 Apr. 1997, U.S. Appln. No. 60/047,585 filed on 23 May 1997, U.S. Appln. No. 60/056,881 filed on 22 Aug. 1997, U.S. Appln. No. 60/043,313 filed on 11 Apr. 1997, U.S. Appln. No. 60/047,586 filed on 23 May 1997, U.S. Appln. No. 60/056,909 filed on 22 Aug. 1997, U.S. Appln. No. 60/040,161 filed on 7 Mar. 1997, U.S. Appln. No. 60/047,587 filed on 23 May 1997, U.S. Appln. No. 60/056,879 filed on 22 Aug. 1997, U.S. Appln. No. 60/047,500 filed on 23 May 1997, U.S. Appln. No. 60/056,880 filed on 22 Aug. 1997, U.S. Appln. No. 60/047,584 filed on 23 May 1997, U.S. Appln. No. 60/056,894 filed on 22 Aug. 1997, U.S. Appln. 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No. 60/040,710 filed on 14 Mar. 1997, U.S. Appln. No. 60/050,934 filed on 30 May 1997, U.S. Appln. No. 60/048,100 filed on 30 May 1997, U.S. Appln. No. 60/040,762 filed on 14 Mar. 1997, U.S. Appln. No. 60/048,357 filed on 30 May 1997, U.S. Appln. No. 60/048,189 filed on 30 May 1997, U.S. Appln. No. 60/041,277 filed on 21 Mar. 1997, U.S. Appln. No. 60/048,188 filed on 30 May 1997, U.S. Appln. No. 60/048,094 filed on 30 May 1997, U.S. Appln. No. 60/048,350 filed on 30 May 1997, U.S. Appln. No. 60/048,135 filed on 30 May 1997, U.S. Appln. No. 60/042,344 filed on 21 Mar. 1997, U.S. Appln. No. 60/048,187 filed on 30 May 1997, U.S. Appln. No. 60/048,099 filed on 30 May 1997, U.S. Appln. No. 60/050,937 filed on 30 May 1997, U.S. Appln. No. 60/048,352 filed on 30 May 1997, U.S. Appln. No. 60/041,276 filed on 21 Mar. 1997, U.S. Appln. No. 60/048,069 filed on 30 May 1997, U.S. Appln. No. 60/048,131 filed on 30 May 1997, U.S. Appln. No. 60/048,186 filed on 30 May 1997, U.S. Appln. 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No. 60/050,901 filed on 13 Jun. 1997, U.S. Appln. No. 60/058,972 filed on 12 Sep. 1997, U.S. Appln. No. 60/049,609 filed on 13 Jun. 1997, U.S. Appln. No. 60/058,975 filed on 12 Sep. 1997, U.S. Appln. No. 60/048,356 filed on 30 May 1997, U.S. Appln. No. 60/056,296 filed on 29 Aug. 1997, U.S. Appln. No. 60/048,101 filed on 30 May 1997, U.S. Appln. No. 60/056,293 filed on 29 Aug. 1997, U.S. Appln. No. 60/050,935 filed on 30 May 1997, U.S. Appln. No. 60/056,250 filed on 29 Aug. 1997, U.S. Appln. No. 60/049,610 filed on 13 Jun. 1997, U.S. Appln. No. 60/061,060 filed on 2 Oct. 1997, U.S. Appln. No. 60/049,606 filed on 13 Jun. 1997, U.S. Appln. No. 60/060,841 filed on 2 Oct. 1997, U.S. Appln. No. 60/049,550 filed on 13 Jun. 1997, U.S. Appln. No. 60/060,834 filed on 2 Oct. 1997, U.S. Appln. No. 60/049,549 filed on 13 Jun. 1997, U.S. Appln. No. 60/060,865 filed on 2 Oct. 1997, U.S. Appln. No. 60/049,548 filed on 13 Jun. 1997, U.S. Appln. No. 60/060,844 filed on 2 Oct. 1997, U.S. Appln. 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No. US01/11988 filed on 12 Apr. 2001, U.S. application Ser. No. 10/100,683 filed 19 Mar. 2002, PCT Appln. No. US02/08278 filed on 19 Mar. 2002, PCT Appln. No. US02/08279 filed on 19 Mar. 2002, PCT Appln. No. US02/08123 filed on 19 Mar. 2002, PCT Appln. No. US02/09785 filed on 19 Mar. 2002, PCT Appln. No. US02/08276 filed on 19 Mar. 2002, PCT Appln. No. US02/08277 filed on 19 Mar. 2002, and PCT Appln. No. US02/08124 filed on 19 Mar. 2002. LENGTHY TABLE The patent application contains a lengthy table section. A copy of the table is available in electronic form from the USPTO web site (http://seqdata.uspto.gov/?pageRequest=docDetail&DocID=US20080103090A1). An electronic copy of the table will also be available from the USPTO upon request and payment of the fee set forth in 37 CFR 1.19(b)(3). 

1. An isolated nucleic acid molecule comprising a first polynucleotide sequence at least 95% identical to a second polynucleotide sequence selected from the group consisting of: (a) a polynucleotide fragment of SEQ ID NO:X as referenced in Table 1A; (b) a polynucleotide encoding a full length polypeptide of SEQ ID NO:Y or a full length polypeptide encoded by the cDNA Clone ID in ATCC Deposit No:Z corresponding to SEQ ID NO:Y as referenced in Table 1A; (c) a polynucleotide encoding a polypeptide fragment of SEQ ID NO:Y or a polypeptide fragment encoded by the cDNA Clone ID in ATCC Deposit No:Z corresponding to SEQ ID NO:Y as referenced in Table 1A; (d) a polynucleotide encoding a polypeptide fragment of SEQ ID NO:Y or a polypeptide fragment encoded by the cDNA Clone ID in ATCC Deposit No:Z corresponding to SEQ ID NO:Y as referenced in Table 1A, wherein said fragment has biological activity; (e) a polynucleotide encoding a polypeptide domain of SEQ ID NO:Y as referenced in Table 1B; (f) a polynucleotide encoding a polypeptide domain of SEQ ID NO:Y as referenced in Table 2; (g) a polynucleotide encoding a predicted epitope of SEQ ID NO:Y as referenced in Table 1B; and (h) a polynucleotide capable of hybridizing under stringent conditions to any one of the polynucleotides specified in (a)-(g), wherein said polynucleotide does not hybridize under stringent conditions to a nucleic acid molecule having a nucleotide sequence of only A residues or of only T residues.
 2. The isolated nucleic acid molecule of claim 1, wherein the polynucleotide fragment comprises a nucleotide sequence encoding a secreted form of SEQ ID NO:Y or a secreted form of the polypeptide encoded by the cDNA Clone ID in ATCC Deposit No:Z corresponding to SEQ ID NO:Y, as referenced in Table 1A.
 3. The isolated nucleic acid molecule of claim 1, wherein the polynucleotide fragment comprises a nucleotide sequence encoding the sequence identified as SEQ ID NO:Y or the polypeptide encoded by the cDNA sequence included in ATCC Deposit No:Z, which is hybridizable to SEQ ID NO:X, as referenced in Table 1A.
 4. The isolated nucleic acid molecule of claim 1, wherein the polynucleotide fragment comprises the entire nucleotide sequence of SEQ ID NO:X or the cDNA sequence included in ATCC Deposit No:Z, which is hybridizable to SEQ ID NO:X, as referenced in Table 1A.
 5. The isolated nucleic acid molecule of claim 2, wherein the nucleotide sequence comprises sequential nucleotide deletions from either the C-terminus or the N-terminus.
 6. The isolated nucleic acid molecule of claim 3, wherein the nucleotide sequence comprises sequential nucleotide deletions from either the C-terminus or the N-terminus.
 7. A recombinant vector comprising the isolated nucleic acid molecule of claim
 1. 8. A method of making a recombinant host cell comprising the isolated nucleic acid molecule of claim
 1. 9. A recombinant host cell produced by the method of claim
 8. 10. The recombinant host cell of claim 9 comprising vector sequences.
 11. A polypeptide comprising a first amino acid sequence at least 95% identical to a second amino acid sequence selected from the group consisting of: (a) a full length polypeptide of SEQ ID NO:Y or a full length polypeptide encoded by the cDNA Clone ID in ATCC Deposit No:Z corresponding to SEQ ID NO:Y as referenced in Table 1A; (b) a secreted form of SEQ ID NO:Y or a secreted form of the polypeptide encoded by the cDNA Clone ID in ATCC Deposit No:Z corresponding to SEQ ID NO:Y as referenced in Table 1A; (c) a polypeptide fragment of SEQ ID NO:Y or a polypeptide fragment encoded by the cDNA Clone ID in ATCC Deposit No:Z corresponding to SEQ ID NO:Y as referenced in Table 1A; (d) a polypeptide fragment of SEQ ID NO:Y or a polypeptide fragment encoded by the cDNA Clone ID in ATCC Deposit No:Z corresponding to SEQ ID NO:Y as referenced in Table 1A, wherein said fragment has biological activity; (e) a polypeptide domain of SEQ ID NO:Y as referenced in Table 1B; (f) a polypeptide domain of SEQ ID NO:Y as referenced in Table 2; and (g) a predicted epitope of SEQ ID NO:Y as referenced in Table 1B.
 12. The polypeptide of claim 11, wherein said polypeptide comprises a heterologous amino acid sequence.
 13. The isolated polypeptide of claim 11, wherein the secreted form or the full length protein comprises sequential amino acid deletions from either the C-terminus or the N-terminus.
 14. An isolated antibody that binds specifically to the isolated polypeptide of claim
 11. 15. A recombinant host cell that expresses the isolated polypeptide of claim
 11. 16. A method of making an isolated polypeptide comprising: (a) culturing the recombinant host cell of claim 15 under conditions such that said polypeptide is expressed; and (b) recovering said polypeptide.
 17. The polypeptide produced by claim
 16. 18. A method for preventing, treating, or ameliorating cancer or other hyperproliferative disorder, comprising administering to a mammalian subject a therapeutically effective amount of the polypeptide of claim
 11. 19. A method of diagnosing cancer or other hyperproliferative disorder in a subject comprising: (a) determining the presence or absence of a mutation in the polynucleotide of claim 11; and (b) diagnosing the cancer or other hyperproliferative disorder based on the presence or absence of said mutation.
 20. A method of diagnosing cancer or other hyperproliferative disorder in a subject comprising: (a) determining the presence or amount of expression of the polypeptide of claim 11 in a biological sample; and (b) diagnosing the cancer or other hyperproliferative disorder based on the presence or amount of expression of the polypeptide.
 21. A method for identifying a binding partner to the polypeptide of claim 11 comprising: (a) contacting the polypeptide of claim 11 with a binding partner; and (b) determining whether the binding partner effects an activity of the polypeptide.
 22. The gene corresponding to the cDNA sequence of SEQ ID NO:X.
 23. A method of identifying an activity in a biological assay, wherein the method comprises: (a) expressing SEQ ID NO:X in a cell; (b) isolating the supernatant; (c) detecting an activity in a biological assay; and (d) identifying the protein in the supernatant having the activity.
 24. The product produced by the method of claim
 20. 